Canonical Allele Identifier: CA2679058227
Gene: RHAG HGNC NCBI

Linked Data

gnomAD v4: 6-49619046-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619046A>T , CM000668.2:g.49619046A>T GRCh38
NC_000006.11:g.49586759A>T , CM000668.1:g.49586759A>T GRCh37
NC_000006.10:g.49694718A>T NCBI36
NG_011704.1:g.22829T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.341+133T>A MANE Select ENSP00000360217.4:n.341+133T>A
ENST00000642530.1:n.616+133T>A
ENST00000646272.1:c.341+133T>A ENSP00000494337.1:n.341+133T>A
ENST00000646939.1:c.341+133T>A ENSP00000494709.1:n.341+133T>A
ENST00000646963.1:c.341+133T>A ENSP00000495337.1:n.341+133T>A
ENST00000229810.9:c.341+133T>A ENSP00000229810.8:n.341+133T>A
ENST00000371175.8:c.341+133T>A ENSP00000360217.4:n.341+133T>A
ENST00000618248.3:c.341+133T>A ENSP00000482984.1:n.341+133T>A
NM_000324.2:c.341+133T>A NP_000315.2:n.341+133T>A
XM_011514788.1:c.341+133T>A XP_011513090.1:n.341+133T>A
NM_000324.3:c.341+133T>A MANE Select NP_000315.2:n.341+133T>A
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