Canonical Allele Identifier: CA1573933696
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661013A= , CM000667.2:g.113661013A= GRCh38
NC_000005.9:g.112996710A= , CM000667.1:g.112996710A= GRCh37
NC_000005.8:g.113024609A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27649A=