Canonical Allele Identifier: CA2658943789

Gene: MSH2

Linked Data

• gnomAD v4: 2-47403041-TCCCACC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47403043_47403048del , CM000664.2:g.47403043_47403048del	GRCh38
NC_000002.11:g.47630182_47630187del , CM000664.1:g.47630182_47630187del	GRCh37
NC_000002.10:g.47483686_47483691del	NCBI36
NG_007110.2:g.4920_4925del , LRG_218:g.4920_4925del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233146.6:c.-149_-144del	ENSP00000233146.2:n.-149_-144del