Product Details

SNP ID

rs200892273

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:186613198 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCAGCTCTGGGGCTGCCACTCAGC[C/G]CCACATGGCCCAGGGCTGATTTATA

Phenotype

MIM: 138680

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

AHSG PubMed Links

Gene Details

Gene

AHSG

Gene Name

alpha 2-HS glycoprotein

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001622.2	271	Silent Mutation	GCC,GCG	A19A	NP_001613.2
XM_017005840.1	271	Silent Mutation	GCC,GCG	A19A	XP_016861329.1

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