Canonical Allele Identifier: CA121295382
Gene: MSH3 HGNC NCBI

Linked Data

dbSNP Id: rs1050041501
MyVariant Identifiers: chr5:g.79971040T>A (hg19) chr5:g.80675221T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80675221T>A , CM000667.2:g.80675221T>A GRCh38
NC_000005.9:g.79971040T>A , CM000667.1:g.79971040T>A GRCh37
NC_000005.8:g.80006796T>A NCBI36
NG_016607.1:g.25747T>A
NG_016607.2:g.25747T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1173+93T>A MANE Select ENSP00000265081.6:n.1173+93T>A
ENST00000658259.1:c.1005+93T>A ENSP00000499617.1:n.1005+93T>A
ENST00000667069.1:c.1173+93T>A ENSP00000499502.1:n.1173+93T>A
ENST00000670357.1:c.1173+93T>A ENSP00000499791.1:n.1173+93T>A
ENST00000265081.6:c.1173+93T>A ENSP00000265081.6:n.1173+93T>A
NM_002439.4:c.1173+93T>A NP_002430.3:n.1173+93T>A
NM_002439.5:c.1173+93T>A MANE Select NP_002430.3:n.1173+93T>A
Search 100 bp 5'
Search 100 bp 3'