Canonical Allele Identifier: CA138848067
Gene: RHAG HGNC NCBI

Linked Data

dbSNP Id: rs952796445
gnomAD v2: 6-49586743-G-A
gnomAD v3: 6-49619030-G-A
gnomAD v4: 6-49619030-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619030G>A , CM000668.2:g.49619030G>A GRCh38
NC_000006.11:g.49586743G>A , CM000668.1:g.49586743G>A GRCh37
NC_000006.10:g.49694702G>A NCBI36
NG_011704.1:g.22845C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.341+149C>T MANE Select ENSP00000360217.4:n.341+149C>T
ENST00000642530.1:n.616+149C>T
ENST00000646272.1:c.341+149C>T ENSP00000494337.1:n.341+149C>T
ENST00000646939.1:c.341+149C>T ENSP00000494709.1:n.341+149C>T
ENST00000646963.1:c.341+149C>T ENSP00000495337.1:n.341+149C>T
ENST00000229810.9:c.341+149C>T ENSP00000229810.8:n.341+149C>T
ENST00000371175.8:c.341+149C>T ENSP00000360217.4:n.341+149C>T
ENST00000618248.3:c.341+149C>T ENSP00000482984.1:n.341+149C>T
NM_000324.2:c.341+149C>T NP_000315.2:n.341+149C>T
XM_011514788.1:c.341+149C>T XP_011513090.1:n.341+149C>T
NM_000324.3:c.341+149C>T MANE Select NP_000315.2:n.341+149C>T