Canonical Allele Identifier: CA364403876
Gene: RHAG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619360A>C , CM000668.2:g.49619360A>C GRCh38
NC_000006.11:g.49587073A>C , CM000668.1:g.49587073A>C GRCh37
NC_000006.10:g.49695032A>C NCBI36
NG_011704.1:g.22515T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.160T>G MANE Select ENSP00000360217.4:p.Phe54Val
ENST00000642530.1:n.435T>G
ENST00000646272.1:c.160T>G ENSP00000494337.1:p.Phe54Val
ENST00000646939.1:c.160T>G ENSP00000494709.1:p.Phe54Val
ENST00000646963.1:c.160T>G ENSP00000495337.1:p.Phe54Val
ENST00000229810.9:c.160T>G ENSP00000229810.8:p.Phe54Val
ENST00000371175.8:c.160T>G ENSP00000360217.4:p.Phe54Val
ENST00000618248.3:c.160T>G ENSP00000482984.1:p.Phe54Val
NM_000324.2:c.160T>G NP_000315.2:p.Phe54Val
XM_011514788.1:c.160T>G XP_011513090.1:p.Phe54Val
NM_000324.3:c.160T>G MANE Select NP_000315.2:p.Phe54Val