Canonical Allele Identifier: CA1691656444
Gene:

Linked Data

dbSNP Id: rs1803285696

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957849C>A , CM000669.2:g.17957849C>A GRCh38
NC_000007.13:g.17997472C>A , CM000669.1:g.17997472C>A GRCh37
NC_000007.12:g.17963997C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-821C>A