Canonical Allele Identifier: CA1264999446
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.81645800A= , CM000664.2:g.81645800A= GRCh38
NC_000002.11:g.81872924A= , CM000664.1:g.81872924A= GRCh37
NC_000002.10:g.81726435A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940294.1:n.563+66191A=
XR_940295.1:n.485+97053A=
XR_001739571.1:n.485+97053A=