Canonical Allele Identifier: CA2713834788
Gene:

Linked Data

dbSNP Id: rs753710529

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957863T>A , CM000669.2:g.17957863T>A GRCh38
NC_000007.13:g.17997486T>A , CM000669.1:g.17997486T>A GRCh37
NC_000007.12:g.17964011T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927078.1:n.271-807T>A