Canonical Allele Identifier: CA375116516
Gene: DOLK HGNC NCBI

Linked Data

ClinVar Variation Id: 2155082
ClinVar RCV Id: RCV003089305
dbSNP Id: rs1324713631
gnomAD v4: 9-128945848-A-T
MyVariant Identifiers: chr9:g.131708127A>T (hg19) chr9:g.128945848A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945848A>T , CM000671.2:g.128945848A>T GRCh38
NC_000009.11:g.131708127A>T , CM000671.1:g.131708127A>T GRCh37
NC_000009.10:g.130747948A>T NCBI36
NG_017009.1:g.6886T>A , LRG_744:g.6886T>A
NG_033111.1:g.3156A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1456T>A MANE Select ENSP00000361667.3:p.Ser486Thr
ENST00000372586.3:c.1456T>A ENSP00000361667.3:p.Ser486Thr
ENST00000482796.1:c.39-3341A>T ENSP00000417556.2:n.39-3341A>T
NM_014908.3:c.1456T>A , LRG_744t1:c.1456T>A NP_055723.1:p.Ser486Thr
NM_014908.4:c.1456T>A MANE Select NP_055723.1:p.Ser486Thr
Search 100 bp 5'
Search 100 bp 3'