Canonical Allele Identifier: CA200444065
Gene: DOLK HGNC NCBI

Linked Data

dbSNP Id: rs755480799
MyVariant Identifiers: chr9:g.131707940C>T (hg19) chr9:g.128945661C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128945661C>T , CM000671.2:g.128945661C>T GRCh38
NC_000009.11:g.131707940C>T , CM000671.1:g.131707940C>T GRCh37
NC_000009.10:g.130747761C>T NCBI36
NG_017009.1:g.7073G>A , LRG_744:g.7073G>A
NG_033111.1:g.2969C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.*26G>A MANE Select ENSP00000361667.3:n.*26G>A
ENST00000372586.3:c.*26G>A ENSP00000361667.3:n.*26G>A
ENST00000482796.1:c.39-3528C>T ENSP00000417556.2:n.39-3528C>T
NM_014908.3:c.*26G>A , LRG_744t1:c.*26G>A NP_055723.1:n.*26G>A
NM_014908.4:c.*26G>A MANE Select NP_055723.1:n.*26G>A
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