Canonical Allele Identifier: CA2658943750
Gene: MSH2 HGNC NCBI

Linked Data

gnomAD v4: 2-47403032-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47403032G>T , CM000664.2:g.47403032G>T GRCh38
NC_000002.11:g.47630171G>T , CM000664.1:g.47630171G>T GRCh37
NC_000002.10:g.47483675G>T NCBI36
NG_007110.2:g.4909G>T , LRG_218:g.4909G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000233146.6:c.-160G>T ENSP00000233146.2:n.-160G>T