Canonical Allele Identifier: CA1558492960
Gene: MSH3 HGNC NCBI

Linked Data

dbSNP Id: rs1749802420
gnomAD v4: 5-80674863-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674863A>T , CM000667.2:g.80674863A>T GRCh38
NC_000005.9:g.79970682A>T , CM000667.1:g.79970682A>T GRCh37
NC_000005.8:g.80006438A>T NCBI36
NG_016607.1:g.25389A>T
NG_016607.2:g.25389A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1028-120A>T MANE Select ENSP00000265081.6:n.1028-120A>T
ENST00000658259.1:c.860-120A>T ENSP00000499617.1:n.860-120A>T
ENST00000667069.1:c.1028-120A>T ENSP00000499502.1:n.1028-120A>T
ENST00000670357.1:c.1028-120A>T ENSP00000499791.1:n.1028-120A>T
ENST00000265081.6:c.1028-120A>T ENSP00000265081.6:n.1028-120A>T
NM_002439.4:c.1028-120A>T NP_002430.3:n.1028-120A>T
NM_002439.5:c.1028-120A>T MANE Select NP_002430.3:n.1028-120A>T
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