Canonical Allele Identifier: CA1481407253
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501153C= , CM000666.2:g.102501153C= GRCh38
NC_000004.11:g.103422310C= , CM000666.1:g.103422310C= GRCh37
NC_000004.10:g.103641342C= NCBI36
NG_050628.1:g.4825C=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+96G= XP_011530769.1:n.643+96G=
NR_136202.1:n.48+1286G=