Canonical Allele Identifier: CA385676098

Gene: MSRB3

Linked Data

• MyVariant Identifiers: chr12:g.65722364T>C (hg19) ; chr12:g.65328584T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65328584T>C , CM000674.2:g.65328584T>C	GRCh38
NC_000012.11:g.65722364T>C , CM000674.1:g.65722364T>C	GRCh37
NC_000012.10:g.64008631T>C	NCBI36
NG_023441.1:g.54942T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000308259.10:c.244T>C MANE Select	ENSP00000312274.6:p.Cys82Arg
ENST00000355192.8:c.265T>C	ENSP00000347324.3:p.Cys89Arg
ENST00000642404.1:c.244T>C	ENSP00000496008.1:p.Cys82Arg
ENST00000642411.1:c.244T>C	ENSP00000494265.1:p.Cys82Arg
ENST00000646299.1:c.244T>C	ENSP00000494941.1:p.Cys82Arg
ENST00000647481.1:c.49T>C	ENSP00000496162.1:p.Cys17Arg
ENST00000308259.9:c.244T>C	ENSP00000312274.5:p.Cys82Arg
ENST00000355192.7:c.265T>C	ENSP00000347324.3:p.Cys89Arg
ENST00000446731.2:c.119T>C
ENST00000535239.5:c.244T>C	ENSP00000445843.1:p.Cys82Arg
ENST00000535664.5:c.244T>C	ENSP00000441650.1:p.Cys82Arg
ENST00000538045.5:c.244T>C	ENSP00000442620.1:p.Cys82Arg
ENST00000540804.5:c.265T>C	ENSP00000437623.1:p.Cys89Arg
ENST00000541189.5:c.290T>C
ENST00000541897.5:c.*89+19929T>C	ENSP00000445051.1:n.*89+19929T>C
ENST00000614640.4:c.244T>C	ENSP00000481483.1:p.Cys82Arg
NM_001031679.2:c.244T>C	NP_001026849.1:p.Cys82Arg
NM_001193460.1:c.244T>C	NP_001180389.1:p.Cys82Arg
NM_001193461.1:c.244T>C	NP_001180390.1:p.Cys82Arg
NM_198080.3:c.265T>C	NP_932346.1:p.Cys89Arg
XM_024448918.1:c.244T>C	XP_024304686.1:p.Cys82Arg
XM_024448919.1:c.244T>C	XP_024304687.1:p.Cys82Arg
XM_024448920.1:c.244T>C	XP_024304688.1:p.Cys82Arg
XM_024448921.1:c.244T>C	XP_024304689.1:p.Cys82Arg
XM_024448922.1:c.397T>C	XP_024304690.1:p.Cys133Arg
NM_001031679.3:c.244T>C MANE Select	NP_001026849.1:p.Cys82Arg
NM_001193460.2:c.244T>C	NP_001180389.1:p.Cys82Arg
NM_198080.4:c.265T>C	NP_932346.1:p.Cys89Arg
NM_001193461.2:c.244T>C	NP_001180390.1:p.Cys82Arg