Canonical Allele Identifier: CA1481407012
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500994G= , CM000666.2:g.102500994G= GRCh38
NC_000004.11:g.103422151G= , CM000666.1:g.103422151G= GRCh37
NC_000004.10:g.103641183G= NCBI36
NG_050628.1:g.4666G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+255C= XP_011530769.1:n.643+255C=
NR_136202.1:n.48+1445C=