Canonical Allele Identifier: CA2496037703

Gene: MSH6

Linked Data

• dbSNP Id: rs1668081989
• gnomAD v4: 2-47782932-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47782932T>C , CM000664.2:g.47782932T>C	GRCh38
NC_000002.11:g.48010071T>C , CM000664.1:g.48010071T>C	GRCh37
NC_000002.10:g.47863575T>C	NCBI36
NG_007111.1:g.4786T>C , LRG_219:g.4786T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7995T>C	ENSP00000498629.1:n.-37-7995T>C
ENST00000606499.1:c.-37-7995T>C	ENSP00000475605.1:n.-37-7995T>C