Canonical Allele Identifier: CA3327782
Gene: MSH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1090191
ClinVar RCV Id: RCV001409261
dbSNP Id: rs774961818
ExAC: 5:79970797 A / G
gnomAD v2: 5-79970797-A-G
gnomAD v4: 5-80674978-A-G
MyVariant Identifiers: chr5:g.79970797A>G (hg19) chr5:g.80674978A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80674978A>G , CM000667.2:g.80674978A>G GRCh38
NC_000005.9:g.79970797A>G , CM000667.1:g.79970797A>G GRCh37
NC_000005.8:g.80006553A>G NCBI36
NG_016607.1:g.25504A>G
NG_016607.2:g.25504A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.1028-5A>G MANE Select ENSP00000265081.6:n.1028-5A>G
ENST00000658259.1:c.860-5A>G ENSP00000499617.1:n.860-5A>G
ENST00000667069.1:c.1028-5A>G ENSP00000499502.1:n.1028-5A>G
ENST00000670357.1:c.1028-5A>G ENSP00000499791.1:n.1028-5A>G
ENST00000265081.6:c.1028-5A>G ENSP00000265081.6:n.1028-5A>G
NM_002439.4:c.1028-5A>G NP_002430.3:n.1028-5A>G
NM_002439.5:c.1028-5A>G MANE Select NP_002430.3:n.1028-5A>G
Search 100 bp 5'
Search 100 bp 3'