Product Details

SNP ID

rs4836699

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:130271152 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCATATCAAGAGCACACGCTATCAC[A/G]GTGATGGAACGCTGTTGATGTTAAG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

HMCN2 PubMed Links

Gene Details

Gene

HMCN2

Gene Name

hemicentin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001291815.1		Intron			NP_001278744.1
XM_011518465.2		Intron			XP_011516767.1
XM_011518466.2		Intron			XP_011516768.1
XM_011518467.2		Intron			XP_011516769.1
XM_011518468.2		Intron			XP_011516770.1
XM_011518469.2		Intron			XP_011516771.1
XM_011518470.2		Intron			XP_011516772.1
XM_017014585.1		Intron			XP_016870074.1
XM_017014586.1		Intron			XP_016870075.1

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