Canonical Allele Identifier: CA2042546309
Gene: MSRB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65389598T>A , CM000674.2:g.65389598T>A GRCh38
NC_000012.11:g.65783378T>A , CM000674.1:g.65783378T>A GRCh37
NC_000012.10:g.64069645T>A NCBI36
NG_023441.1:g.115956T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000308259.10:c.292+20572T>A MANE Select ENSP00000312274.6:n.292+20572T>A
ENST00000355192.8:c.313+20572T>A ENSP00000347324.3:n.313+20572T>A
ENST00000642404.1:c.292+20572T>A ENSP00000496008.1:n.292+20572T>A
ENST00000642411.1:c.292+20572T>A ENSP00000494265.1:n.292+20572T>A
ENST00000646299.1:c.292+20572T>A ENSP00000494941.1:n.292+20572T>A
ENST00000647481.1:c.97+20572T>A ENSP00000496162.1:n.97+20572T>A
ENST00000308259.9:c.292+20572T>A ENSP00000312274.5:n.292+20572T>A
ENST00000355192.7:c.313+20572T>A ENSP00000347324.3:n.313+20572T>A
ENST00000446731.2:c.167+20572T>A
ENST00000535143.1:n.131+20572T>A
ENST00000535239.5:c.292+20572T>A ENSP00000445843.1:n.292+20572T>A
ENST00000535664.5:c.292+20572T>A ENSP00000441650.1:n.292+20572T>A
ENST00000538045.5:c.292+20572T>A ENSP00000442620.1:n.292+20572T>A
ENST00000540804.5:c.313+20572T>A ENSP00000437623.1:n.313+20572T>A
ENST00000541189.5:c.338+20572T>A
ENST00000541897.5:c.*118+20572T>A ENSP00000445051.1:n.*118+20572T>A
ENST00000614640.4:c.292+20572T>A ENSP00000481483.1:n.292+20572T>A
NM_001031679.2:c.292+20572T>A NP_001026849.1:n.292+20572T>A
NM_001193460.1:c.292+20572T>A NP_001180389.1:n.292+20572T>A
NM_001193461.1:c.292+20572T>A NP_001180390.1:n.292+20572T>A
NM_198080.3:c.313+20572T>A NP_932346.1:n.313+20572T>A
XM_024448918.1:c.292+20572T>A XP_024304686.1:n.292+20572T>A
XM_024448919.1:c.292+20572T>A XP_024304687.1:n.292+20572T>A
XM_024448920.1:c.292+20572T>A XP_024304688.1:n.292+20572T>A
XM_024448921.1:c.292+20572T>A XP_024304689.1:n.292+20572T>A
NM_001031679.3:c.292+20572T>A MANE Select NP_001026849.1:n.292+20572T>A
NM_001193460.2:c.292+20572T>A NP_001180389.1:n.292+20572T>A
NM_198080.4:c.313+20572T>A NP_932346.1:n.313+20572T>A
NM_001193461.2:c.292+20572T>A NP_001180390.1:n.292+20572T>A