Canonical Allele Identifier: CA2496037720

Gene: MSH6

Linked Data

• dbSNP Id: rs1668083802

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47782952C>G , CM000664.2:g.47782952C>G	GRCh38
NC_000002.11:g.48010091C>G , CM000664.1:g.48010091C>G	GRCh37
NC_000002.10:g.47863595C>G	NCBI36
NG_007111.1:g.4806C>G , LRG_219:g.4806C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-7975C>G	ENSP00000498629.1:n.-37-7975C>G
ENST00000606499.1:c.-37-7975C>G	ENSP00000475605.1:n.-37-7975C>G