Canonical Allele Identifier: CA2496037815
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668092383
gnomAD v4: 2-47783036-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783036T>A , CM000664.2:g.47783036T>A GRCh38
NC_000002.11:g.48010175T>A , CM000664.1:g.48010175T>A GRCh37
NC_000002.10:g.47863679T>A NCBI36
NG_007111.1:g.4890T>A , LRG_219:g.4890T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7891T>A ENSP00000498629.1:n.-37-7891T>A
ENST00000606499.1:c.-37-7891T>A ENSP00000475605.1:n.-37-7891T>A
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