Canonical Allele Identifier: CA1627456331
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636863G= , CM000668.2:g.49636863G= GRCh38
NC_000006.11:g.49604576G= , CM000668.1:g.49604576G= GRCh37
NC_000006.10:g.49712535G= NCBI36
NG_011704.1:g.5012C=

Transcript Alleles

HGVS Amino-acid Change
NM_000324.2:c.-51C= NP_000315.2:n.-51C=
XM_011514788.1:c.-51C= XP_011513090.1:n.-51C=