Canonical Allele Identifier: CA46686926
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs969054394
MyVariant Identifiers: chr2:g.48010115A>C (hg19) chr2:g.47782976A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782976A>C , CM000664.2:g.47782976A>C GRCh38
NC_000002.11:g.48010115A>C , CM000664.1:g.48010115A>C GRCh37
NC_000002.10:g.47863619A>C NCBI36
NG_007111.1:g.4830A>C , LRG_219:g.4830A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7951A>C ENSP00000498629.1:n.-37-7951A>C
ENST00000606499.1:c.-37-7951A>C ENSP00000475605.1:n.-37-7951A>C
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