Canonical Allele Identifier: CA2496037688

Gene: MSH6

Linked Data

• dbSNP Id: rs1668080359

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47782917_47782918insTCCC , CM000664.2:g.47782917_47782918insTCCC	GRCh38
NC_000002.11:g.48010056_48010057insTCCC , CM000664.1:g.48010056_48010057insTCCC	GRCh37
NC_000002.10:g.47863560_47863561insTCCC	NCBI36
NG_007111.1:g.4771_4772insTCCC , LRG_219:g.4771_4772insTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000652107.1:c.-37-8010_-37-8009insTCCC	ENSP00000498629.1:n.-37-8010_-37-8009insTCCC
ENST00000606499.1:c.-37-8010_-37-8009insTCCC	ENSP00000475605.1:n.-37-8010_-37-8009insTCCC