Canonical Allele Identifier: CA360267956
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1412247
ClinVar RCV Id: RCV001919042 RCV002407065
dbSNP Id: rs757051997
MyVariant Identifiers: chr5:g.79970839T>G (hg19) chr5:g.80675020T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80675020T>G , CM000667.2:g.80675020T>G GRCh38
NC_000005.9:g.79970839T>G , CM000667.1:g.79970839T>G GRCh37
NC_000005.8:g.80006595T>G NCBI36
NG_016607.1:g.25546T>G
NG_016607.2:g.25546T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1065T>G MANE Select ENSP00000265081.6:p.Asn355Lys
ENST00000658259.1:c.897T>G ENSP00000499617.1:p.Asn299Lys
ENST00000667069.1:c.1065T>G ENSP00000499502.1:p.Asn355Lys
ENST00000670357.1:c.1065T>G ENSP00000499791.1:p.Asn355Lys
ENST00000265081.6:c.1065T>G ENSP00000265081.6:p.Asn355Lys
NM_002439.4:c.1065T>G NP_002430.3:p.Asn355Lys
NM_002439.5:c.1065T>G MANE Select NP_002430.3:p.Asn355Lys
Search 100 bp 5'
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