Canonical Allele Identifier: CA364403720
Gene: RHAG HGNC NCBI

Linked Data

dbSNP Id: rs745946393
gnomAD v2: 6-49587054-A-G
gnomAD v4: 6-49619341-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49619341A>G , CM000668.2:g.49619341A>G GRCh38
NC_000006.11:g.49587054A>G , CM000668.1:g.49587054A>G GRCh37
NC_000006.10:g.49695013A>G NCBI36
NG_011704.1:g.22534T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371175.10:c.179T>C MANE Select ENSP00000360217.4:p.Met60Thr
ENST00000642530.1:n.454T>C
ENST00000646272.1:c.179T>C ENSP00000494337.1:p.Met60Thr
ENST00000646939.1:c.179T>C ENSP00000494709.1:p.Met60Thr
ENST00000646963.1:c.179T>C ENSP00000495337.1:p.Met60Thr
ENST00000229810.9:c.179T>C ENSP00000229810.8:p.Met60Thr
ENST00000371175.8:c.179T>C ENSP00000360217.4:p.Met60Thr
ENST00000618248.3:c.179T>C ENSP00000482984.1:p.Met60Thr
NM_000324.2:c.179T>C NP_000315.2:p.Met60Thr
XM_011514788.1:c.179T>C XP_011513090.1:p.Met60Thr
NM_000324.3:c.179T>C MANE Select NP_000315.2:p.Met60Thr