Canonical Allele Identifier: CA1481405740
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499820G= , CM000666.2:g.102499820G= GRCh38
NC_000004.11:g.103420977G= , CM000666.1:g.103420977G= GRCh37
NC_000004.10:g.103640009G= NCBI36
NG_050628.1:g.3492G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1429C= XP_011530769.1:n.643+1429C=
NR_136202.1:n.48+2619C=