Canonical Allele Identifier: CA1481407071
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501028G= , CM000666.2:g.102501028G= GRCh38
NC_000004.11:g.103422185G= , CM000666.1:g.103422185G= GRCh37
NC_000004.10:g.103641217G= NCBI36
NG_050628.1:g.4700G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+221C= XP_011530769.1:n.643+221C=
NR_136202.1:n.48+1411C=