Canonical Allele Identifier: CA2580066639

Gene: MSH2

Linked Data

• ClinVar Variation Id: 1782645
• ClinVar RCV Id: RCV002410678
• dbSNP Id: rs2103855893

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403001G>A , CM000664.2:g.47403001G>A	GRCh38
NC_000002.11:g.47630140G>A , CM000664.1:g.47630140G>A	GRCh37
NC_000002.10:g.47483644G>A	NCBI36
NG_007110.2:g.4878G>A , LRG_218:g.4878G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-191G>A	ENSP00000233146.2:n.-191G>A