Canonical Allele Identifier: CA2496037834
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668093580
gnomAD v4: 2-47783054-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783054C>G , CM000664.2:g.47783054C>G GRCh38
NC_000002.11:g.48010193C>G , CM000664.1:g.48010193C>G GRCh37
NC_000002.10:g.47863697C>G NCBI36
NG_007111.1:g.4908C>G , LRG_219:g.4908C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7873C>G ENSP00000498629.1:n.-37-7873C>G
ENST00000606499.1:c.-37-7873C>G ENSP00000475605.1:n.-37-7873C>G