Canonical Allele Identifier: CA2699073700

Gene: MSH2

Linked Data

• dbSNP Id: rs17224101

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403031C>G , CM000664.2:g.47403031C>G	GRCh38
NC_000002.11:g.47630170C>G , CM000664.1:g.47630170C>G	GRCh37
NC_000002.10:g.47483674C>G	NCBI36
NG_007110.2:g.4908C>G , LRG_218:g.4908C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-161C>G	ENSP00000233146.2:n.-161C>G