Canonical Allele Identifier: CA375118997
Gene: DOLK HGNC NCBI

Linked Data

ClinVar Variation Id: 1018123
ClinVar RCV Id: RCV001317379
dbSNP Id: rs1841659405
MyVariant Identifiers: chr9:g.131708356G>C (hg19) chr9:g.128946077G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.128946077G>C , CM000671.2:g.128946077G>C GRCh38
NC_000009.11:g.131708356G>C , CM000671.1:g.131708356G>C GRCh37
NC_000009.10:g.130748177G>C NCBI36
NG_017009.1:g.6657C>G , LRG_744:g.6657C>G
NG_033111.1:g.3385G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372586.4:c.1227C>G MANE Select ENSP00000361667.3:p.Ile409Met
ENST00000372586.3:c.1227C>G ENSP00000361667.3:p.Ile409Met
ENST00000482796.1:c.39-3112G>C ENSP00000417556.2:n.39-3112G>C
NM_014908.3:c.1227C>G , LRG_744t1:c.1227C>G NP_055723.1:p.Ile409Met
NM_014908.4:c.1227C>G MANE Select NP_055723.1:p.Ile409Met
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