Canonical Allele Identifier: CA1627456307
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636842G= , CM000668.2:g.49636842G= GRCh38
NC_000006.11:g.49604555G= , CM000668.1:g.49604555G= GRCh37
NC_000006.10:g.49712514G= NCBI36
NG_011704.1:g.5033C=

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-30C= NP_000315.2:n.-30C=
XM_011514788.1:c.-30C= XP_011513090.1:n.-30C=