Product Details

SNP ID

rs1477941

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.18:11692441 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGAGCGGTAGCAGAGCTCTCCCCT[C/G]CAGTGCTCACCTCCAGAATATCGCA

Phenotype

MIM: 139312

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

GNAL PubMed Links

Gene Details

Gene

GNAL

Gene Name

G protein subunit alpha L

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142339.2		Intron			NP_001135811.1
NM_001261443.1		Intron			NP_001248372.1
NM_001261444.1		Intron			NP_001248373.1
NM_182978.3		Intron			NP_892023.1
XM_006722324.2		Intron			XP_006722387.1

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