Canonical Allele Identifier: CA385671524

Gene: MSRB3

Linked Data

• MyVariant Identifiers: chr12:g.65702426C>G (hg19) ; chr12:g.65308646C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65308646C>G , CM000674.2:g.65308646C>G	GRCh38
NC_000012.11:g.65702426C>G , CM000674.1:g.65702426C>G	GRCh37
NC_000012.10:g.63988693C>G	NCBI36
NG_023441.1:g.35004C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000308259.10:c.67C>G MANE Select	ENSP00000312274.6:p.Leu23Val
ENST00000355192.8:c.98-18180C>G	ENSP00000347324.3:n.98-18180C>G
ENST00000642404.1:c.67C>G	ENSP00000496008.1:p.Leu23Val
ENST00000642411.1:c.67C>G	ENSP00000494265.1:p.Leu23Val
ENST00000645872.1:n.407C>G
ENST00000646299.1:c.67C>G	ENSP00000494941.1:p.Leu23Val
ENST00000308259.9:c.67C>G	ENSP00000312274.5:p.Leu23Val
ENST00000355192.7:c.98-18180C>G	ENSP00000347324.3:n.98-18180C>G
ENST00000535239.5:c.67C>G	ENSP00000445843.1:p.Leu23Val
ENST00000535664.5:c.67C>G	ENSP00000441650.1:p.Leu23Val
ENST00000538045.5:c.67C>G	ENSP00000442620.1:p.Leu23Val
ENST00000538725.1:n.280C>G
ENST00000540804.5:c.98-18180C>G	ENSP00000437623.1:n.98-18180C>G
ENST00000541189.5:c.123-18180C>G
ENST00000541897.5:c.*80C>G	ENSP00000445051.1:n.*80C>G
ENST00000614640.4:c.67C>G	ENSP00000481483.1:p.Leu23Val
NM_001031679.2:c.67C>G	NP_001026849.1:p.Leu23Val
NM_001193460.1:c.67C>G	NP_001180389.1:p.Leu23Val
NM_001193461.1:c.67C>G	NP_001180390.1:p.Leu23Val
NM_198080.3:c.98-18180C>G	NP_932346.1:n.98-18180C>G
XM_024448918.1:c.67C>G	XP_024304686.1:p.Leu23Val
XM_024448919.1:c.67C>G	XP_024304687.1:p.Leu23Val
XM_024448920.1:c.67C>G	XP_024304688.1:p.Leu23Val
XM_024448921.1:c.67C>G	XP_024304689.1:p.Leu23Val
XM_024448922.1:c.230-18180C>G	XP_024304690.1:n.230-18180C>G
NM_001031679.3:c.67C>G MANE Select	NP_001026849.1:p.Leu23Val
NM_001193460.2:c.67C>G	NP_001180389.1:p.Leu23Val
NM_198080.4:c.98-18180C>G	NP_932346.1:n.98-18180C>G
NM_001193461.2:c.67C>G	NP_001180390.1:p.Leu23Val