Canonical Allele Identifier: CA1481407422
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501253C= , CM000666.2:g.102501253C= GRCh38
NC_000004.11:g.103422410C= , CM000666.1:g.103422410C= GRCh37
NC_000004.10:g.103641442C= NCBI36
NG_050628.1:g.4925C=

Transcript Alleles

HGVS Amino-acid Change
XM_011532467.1:c.639G= XP_011530769.1:p.Ala213=
NR_136202.1:n.48+1186G=