Canonical Allele Identifier: CA1481405449
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499636A= , CM000666.2:g.102499636A= GRCh38
NC_000004.11:g.103420793A= , CM000666.1:g.103420793A= GRCh37
NC_000004.10:g.103639825A= NCBI36
NG_050628.1:g.3308A=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+1613T= XP_011530769.1:n.643+1613T=
NR_136202.1:n.48+2803T=