Canonical Allele Identifier: CA2658944051
Gene: MSH2 HGNC NCBI

Linked Data

dbSNP Id: rs2103861234
gnomAD v4: 2-47403099-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403099G>C , CM000664.2:g.47403099G>C GRCh38
NC_000002.11:g.47630238G>C , CM000664.1:g.47630238G>C GRCh37
NC_000002.10:g.47483742G>C NCBI36
NG_007110.2:g.4976G>C , LRG_218:g.4976G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000543555.6:c.-107G>C ENSP00000442697.1:n.-107G>C
ENST00000233146.6:c.-93G>C ENSP00000233146.2:n.-93G>C
ENST00000454849.5:c.-107G>C ENSP00000411482.1:n.-107G>C
ENST00000543555.5:c.-107G>C ENSP00000442697.1:n.-107G>C
NM_000251.2:c.-93G>C , LRG_218t1:c.-93G>C NP_000242.1:n.-93G>C
NM_001258281.1:c.-107G>C NP_001245210.1:n.-107G>C
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