Canonical Allele Identifier: CA1481405751
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499830G= , CM000666.2:g.102499830G= GRCh38
NC_000004.11:g.103420987G= , CM000666.1:g.103420987G= GRCh37
NC_000004.10:g.103640019G= NCBI36
NG_050628.1:g.3502G=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1419C= XP_011530769.1:n.643+1419C=
NR_136202.1:n.48+2609C=