Canonical Allele Identifier: CA814453566
Gene: MSH3 HGNC NCBI

Linked Data

dbSNP Id: rs1207082559
MyVariant Identifiers: chr5:g.79970647C>G (hg19) chr5:g.80674828C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674828C>G , CM000667.2:g.80674828C>G GRCh38
NC_000005.9:g.79970647C>G , CM000667.1:g.79970647C>G GRCh37
NC_000005.8:g.80006403C>G NCBI36
NG_016607.1:g.25354C>G
NG_016607.2:g.25354C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1028-155C>G MANE Select ENSP00000265081.6:n.1028-155C>G
ENST00000658259.1:c.860-155C>G ENSP00000499617.1:n.860-155C>G
ENST00000667069.1:c.1028-155C>G ENSP00000499502.1:n.1028-155C>G
ENST00000670357.1:c.1028-155C>G ENSP00000499791.1:n.1028-155C>G
ENST00000265081.6:c.1028-155C>G ENSP00000265081.6:n.1028-155C>G
NM_002439.4:c.1028-155C>G NP_002430.3:n.1028-155C>G
NM_002439.5:c.1028-155C>G MANE Select NP_002430.3:n.1028-155C>G
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