Canonical Allele Identifier: CA1627456310
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49636845C= , CM000668.2:g.49636845C= GRCh38
NC_000006.11:g.49604558C= , CM000668.1:g.49604558C= GRCh37
NC_000006.10:g.49712517C= NCBI36
NG_011704.1:g.5030G=

Transcript Alleles

HGVS Amino-acid change
NM_000324.2:c.-33G= NP_000315.2:n.-33G=
XM_011514788.1:c.-33G= XP_011513090.1:n.-33G=