Canonical Allele Identifier: CA1627456313
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636849A= , CM000668.2:g.49636849A= GRCh38
NC_000006.11:g.49604562A= , CM000668.1:g.49604562A= GRCh37
NC_000006.10:g.49712521A= NCBI36
NG_011704.1:g.5026T=

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-37T= NP_000315.2:n.-37T=
XM_011514788.1:c.-37T= XP_011513090.1:n.-37T=