Canonical Allele Identifier: CA1627477927
Gene: RHAG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619148C= , CM000668.2:g.49619148C= GRCh38
NC_000006.11:g.49586861C= , CM000668.1:g.49586861C= GRCh37
NC_000006.10:g.49694820C= NCBI36
NG_011704.1:g.22727G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.341+31G= MANE Select ENSP00000360217.4:n.341+31G=
ENST00000642530.1:n.616+31G=
ENST00000646272.1:c.341+31G= ENSP00000494337.1:n.341+31G=
ENST00000646939.1:c.341+31G= ENSP00000494709.1:n.341+31G=
ENST00000646963.1:c.341+31G= ENSP00000495337.1:n.341+31G=
ENST00000229810.9:c.341+31G= ENSP00000229810.8:n.341+31G=
ENST00000371175.8:c.341+31G= ENSP00000360217.4:n.341+31G=
ENST00000618248.3:c.341+31G= ENSP00000482984.1:n.341+31G=
NM_000324.2:c.341+31G= NP_000315.2:n.341+31G=
XM_011514788.1:c.341+31G= XP_011513090.1:n.341+31G=
NM_000324.3:c.341+31G= MANE Select NP_000315.2:n.341+31G=
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