Canonical Allele Identifier: CA1481405429
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499624G= , CM000666.2:g.102499624G= GRCh38
NC_000004.11:g.103420781G= , CM000666.1:g.103420781G= GRCh37
NC_000004.10:g.103639813G= NCBI36
NG_050628.1:g.3296G=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1625C= XP_011530769.1:n.643+1625C=
NR_136202.1:n.48+2815C=