Canonical Allele Identifier: CA816711681
Gene:

Linked Data

dbSNP Id: rs1301467316

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105805177T>C , CM000668.2:g.105805177T>C GRCh38
NC_000006.11:g.106253052T>C , CM000668.1:g.106253052T>C GRCh37
NC_000006.10:g.106359745T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942835.1:n.510+24880A>G
XR_001744274.1:n.438+24880A>G
XR_001744275.1:n.337+24880A>G