Canonical Allele Identifier: CA46665924

Gene: MSH2

Linked Data

• dbSNP Id: rs987459306
• MyVariant Identifiers: chr2:g.47630124C>G (hg19) ; chr2:g.47402985C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47402985C>G , CM000664.2:g.47402985C>G	GRCh38
NC_000002.11:g.47630124C>G , CM000664.1:g.47630124C>G	GRCh37
NC_000002.10:g.47483628C>G	NCBI36
NG_007110.2:g.4862C>G , LRG_218:g.4862C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-207C>G	ENSP00000233146.2:n.-207C>G