Canonical Allele Identifier: CA445159952
Gene: MSH3 HGNC NCBI

Linked Data

dbSNP Id: rs2112816134
MyVariant Identifiers: chr5:g.79970941C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80675122C>A , CM000667.2:g.80675122C>A GRCh38
NC_000005.9:g.79970941C>A , CM000667.1:g.79970941C>A GRCh37
NC_000005.8:g.80006697C>A NCBI36
NG_016607.1:g.25648C>A
NG_016607.2:g.25648C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1167C>A MANE Select ENSP00000265081.6:p.Gly389=
ENST00000658259.1:c.999C>A ENSP00000499617.1:p.Gly333=
ENST00000667069.1:c.1167C>A ENSP00000499502.1:p.Gly389=
ENST00000670357.1:c.1167C>A ENSP00000499791.1:p.Gly389=
ENST00000265081.6:c.1167C>A ENSP00000265081.6:p.Gly389=
NM_002439.4:c.1167C>A NP_002430.3:p.Gly389=
NM_002439.5:c.1167C>A MANE Select NP_002430.3:p.Gly389=
Search 100 bp 5'
Search 100 bp 3'