Canonical Allele Identifier: CA364398140

Gene: RHAG

Linked Data

• gnomAD v4: 6-49612410-T-C
• MyVariant Identifiers: chr6:g.49580123T>C (hg19) ; chr6:g.49612410T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49612410T>C , CM000668.2:g.49612410T>C	GRCh38
NC_000006.11:g.49580123T>C , CM000668.1:g.49580123T>C	GRCh37
NC_000006.10:g.49688082T>C	NCBI36
NG_011704.1:g.29465A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371175.10:c.932A>G MANE Select	ENSP00000360217.4:p.Tyr311Cys
ENST00000646272.1:c.932A>G	ENSP00000494337.1:p.Tyr311Cys
ENST00000646874.1:n.622A>G
ENST00000646939.1:c.932A>G	ENSP00000494709.1:p.Tyr311Cys
ENST00000646963.1:c.932A>G	ENSP00000495337.1:p.Tyr311Cys
ENST00000229810.9:c.932A>G	ENSP00000229810.8:p.Tyr311Cys
ENST00000371175.8:c.932A>G	ENSP00000360217.4:p.Tyr311Cys
ENST00000618248.3:c.932A>G	ENSP00000482984.1:p.Tyr311Cys
NM_000324.2:c.932A>G	NP_000315.2:p.Tyr311Cys
NM_000324.3:c.932A>G MANE Select	NP_000315.2:p.Tyr311Cys