Canonical Allele Identifier: CA14453386
Gene:

Linked Data

dbSNP Id: rs7210086

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.72645559A>C , CM000679.2:g.72645559A>C GRCh38
NC_000017.10:g.70641698A>C , CM000679.1:g.70641698A>C GRCh37
NC_000017.9:g.68153293A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001752993.1:n.2278A>C
XR_934960.2:n.2480A>C
XR_934961.2:n.2268A>C