Canonical Allele Identifier: CA1481407417
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102501249C= , CM000666.2:g.102501249C= GRCh38
NC_000004.11:g.103422406C= , CM000666.1:g.103422406C= GRCh37
NC_000004.10:g.103641438C= NCBI36
NG_050628.1:g.4921C=

Transcript Alleles

HGVS Amino-acid change
XM_011532467.1:c.643G= XP_011530769.1:p.Asp215=
NR_136202.1:n.48+1190G=