Canonical Allele Identifier: CA138848023

Gene: RHAG

Linked Data

• dbSNP Id: rs147563393
• gnomAD v2: 6-49586641-T-G
• gnomAD v3: 6-49618928-T-G
• gnomAD v4: 6-49618928-T-G
• MyVariant Identifiers: chr6:g.49586641T>G (hg19) ; chr6:g.49618928T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49618928T>G , CM000668.2:g.49618928T>G	GRCh38
NC_000006.11:g.49586641T>G , CM000668.1:g.49586641T>G	GRCh37
NC_000006.10:g.49694600T>G	NCBI36
NG_011704.1:g.22947A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371175.10:c.341+251A>C MANE Select	ENSP00000360217.4:n.341+251A>C
ENST00000642530.1:n.616+251A>C
ENST00000646272.1:c.341+251A>C	ENSP00000494337.1:n.341+251A>C
ENST00000646939.1:c.341+251A>C	ENSP00000494709.1:n.341+251A>C
ENST00000646963.1:c.341+251A>C	ENSP00000495337.1:n.341+251A>C
ENST00000229810.9:c.341+251A>C	ENSP00000229810.8:n.341+251A>C
ENST00000371175.8:c.341+251A>C	ENSP00000360217.4:n.341+251A>C
ENST00000618248.3:c.341+251A>C	ENSP00000482984.1:n.341+251A>C
NM_000324.2:c.341+251A>C	NP_000315.2:n.341+251A>C
XM_011514788.1:c.341+251A>C	XP_011513090.1:n.341+251A>C
NM_000324.3:c.341+251A>C MANE Select	NP_000315.2:n.341+251A>C