Canonical Allele Identifier: CA1481405811
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499870T= , CM000666.2:g.102499870T= GRCh38
NC_000004.11:g.103421027T= , CM000666.1:g.103421027T= GRCh37
NC_000004.10:g.103640059T= NCBI36
NG_050628.1:g.3542T=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1379A= XP_011530769.1:n.643+1379A=
NR_136202.1:n.48+2569A=