Canonical Allele Identifier: CA1627469216
Gene: RHAG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49612518G= , CM000668.2:g.49612518G= GRCh38
NC_000006.11:g.49580231G= , CM000668.1:g.49580231G= GRCh37
NC_000006.10:g.49688190G= NCBI36
NG_011704.1:g.29357C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.824C= MANE Select ENSP00000360217.4:p.Ala275=
ENST00000646272.1:c.824C= ENSP00000494337.1:p.Ala275=
ENST00000646874.1:n.514C=
ENST00000646939.1:c.824C= ENSP00000494709.1:p.Ala275=
ENST00000646963.1:c.824C= ENSP00000495337.1:p.Ala275=
ENST00000229810.9:c.824C= ENSP00000229810.8:p.Ala275=
ENST00000371175.8:c.824C= ENSP00000360217.4:p.Ala275=
ENST00000618248.3:c.824C= ENSP00000482984.1:p.Ala275=
NM_000324.2:c.824C= NP_000315.2:p.Ala275=
NM_000324.3:c.824C= MANE Select NP_000315.2:p.Ala275=