Canonical Allele Identifier: CA360267869
Gene: MSH3 HGNC NCBI

Linked Data

dbSNP Id: rs2112815933
MyVariant Identifiers: chr5:g.79970817T>A (hg19) chr5:g.80674998T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674998T>A , CM000667.2:g.80674998T>A GRCh38
NC_000005.9:g.79970817T>A , CM000667.1:g.79970817T>A GRCh37
NC_000005.8:g.80006573T>A NCBI36
NG_016607.1:g.25524T>A
NG_016607.2:g.25524T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1043T>A MANE Select ENSP00000265081.6:p.Ile348Asn
ENST00000658259.1:c.875T>A ENSP00000499617.1:p.Ile292Asn
ENST00000667069.1:c.1043T>A ENSP00000499502.1:p.Ile348Asn
ENST00000670357.1:c.1043T>A ENSP00000499791.1:p.Ile348Asn
ENST00000265081.6:c.1043T>A ENSP00000265081.6:p.Ile348Asn
NM_002439.4:c.1043T>A NP_002430.3:p.Ile348Asn
NM_002439.5:c.1043T>A MANE Select NP_002430.3:p.Ile348Asn
Search 100 bp 5'
Search 100 bp 3'