Canonical Allele Identifier: CA1481406882
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102500926G= , CM000666.2:g.102500926G= GRCh38
NC_000004.11:g.103422083G= , CM000666.1:g.103422083G= GRCh37
NC_000004.10:g.103641115G= NCBI36
NG_050628.1:g.4598G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+323C= XP_011530769.1:n.643+323C=
NR_136202.1:n.48+1513C=