Canonical Allele Identifier: CA781922710

Gene: DOK6

Linked Data

• dbSNP Id: rs1373693521
• MyVariant Identifiers: chr18:g.67283172C>T (hg19) ; chr18:g.69615936C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.69615936C>T , CM000680.2:g.69615936C>T	GRCh38
NC_000018.9:g.67283172C>T , CM000680.1:g.67283172C>T	GRCh37
NC_000018.8:g.65434152C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000382713.10:c.289+16438C>T MANE Select	ENSP00000372160.5:n.289+16438C>T
ENST00000382713.9:c.289+16438C>T	ENSP00000372160.5:n.289+16438C>T
NM_152721.5:c.289+16438C>T	NP_689934.2:n.289+16438C>T
XM_011525873.1:c.289+16438C>T	XP_011524175.1:n.289+16438C>T
XM_011525874.1:c.289+16438C>T	XP_011524176.1:n.289+16438C>T
XM_011525875.1:c.289+16438C>T	XP_011524177.1:n.289+16438C>T
XM_011525875.2:c.289+16438C>T	XP_011524177.1:n.289+16438C>T
NM_152721.6:c.289+16438C>T MANE Select	NP_689934.2:n.289+16438C>T