Canonical Allele Identifier: CA532704915
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785699
ClinVar RCV Id: RCV002424011
dbSNP Id: rs786202450
gnomAD v2: 2-47630123-A-T
gnomAD v3: 2-47402984-A-T
gnomAD v4: 2-47402984-A-T
MyVariant Identifiers: chr2:g.47630123A>T (hg19) chr2:g.47402984A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47402984A>T , CM000664.2:g.47402984A>T GRCh38
NC_000002.11:g.47630123A>T , CM000664.1:g.47630123A>T GRCh37
NC_000002.10:g.47483627A>T NCBI36
NG_007110.2:g.4861A>T , LRG_218:g.4861A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-208A>T ENSP00000233146.2:n.-208A>T
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