Canonical Allele Identifier: CA2311756659
Gene: DOK6 HGNC NCBI

Linked Data

dbSNP Id: rs1599223413

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.69615747A>C , CM000680.2:g.69615747A>C GRCh38
NC_000018.9:g.67282983A>C , CM000680.1:g.67282983A>C GRCh37
NC_000018.8:g.65433963A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000382713.10:c.289+16249A>C MANE Select ENSP00000372160.5:n.289+16249A>C
ENST00000382713.9:c.289+16249A>C ENSP00000372160.5:n.289+16249A>C
NM_152721.5:c.289+16249A>C NP_689934.2:n.289+16249A>C
XM_011525873.1:c.289+16249A>C XP_011524175.1:n.289+16249A>C
XM_011525874.1:c.289+16249A>C XP_011524176.1:n.289+16249A>C
XM_011525875.1:c.289+16249A>C XP_011524177.1:n.289+16249A>C
XM_011525875.2:c.289+16249A>C XP_011524177.1:n.289+16249A>C
NM_152721.6:c.289+16249A>C MANE Select NP_689934.2:n.289+16249A>C