Canonical Allele Identifier: CA1481407048
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501008C= , CM000666.2:g.102501008C= GRCh38
NC_000004.11:g.103422165C= , CM000666.1:g.103422165C= GRCh37
NC_000004.10:g.103641197C= NCBI36
NG_050628.1:g.4680C=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643+241G= XP_011530769.1:n.643+241G=
NR_136202.1:n.48+1431G=