Canonical Allele Identifier: CA1481405675
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102499759A= , CM000666.2:g.102499759A= GRCh38
NC_000004.11:g.103420916A= , CM000666.1:g.103420916A= GRCh37
NC_000004.10:g.103639948A= NCBI36
NG_050628.1:g.3431A=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.643+1490T= XP_011530769.1:n.643+1490T=
NR_136202.1:n.48+2680T=