Canonical Allele Identifier: CA1373744071
Gene:

Linked Data

dbSNP Id: rs1575679144

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577239T>C , CM000665.2:g.70577239T>C GRCh38
NC_000003.11:g.70626390T>C , CM000665.1:g.70626390T>C GRCh37
NC_000003.10:g.70709080T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.406+1279A>G
XR_001740559.1:n.366+1279A>G