Canonical Allele Identifier: CA9207965
Gene: DOCK6 HGNC NCBI
ANGPTL8 HGNC NCBI

Linked Data

dbSNP Id: rs2278426
ExAC: 19:11350488 C / T
gnomAD v2: 19-11350488-C-T
gnomAD v3: 19-11239812-C-T
gnomAD v4: 19-11239812-C-T
MyVariant Identifiers: chr19:g.11350488C>T (hg19) chr19:g.11239812C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11239812C>T , CM000681.2:g.11239812C>T GRCh38
NC_000019.9:g.11350488C>T , CM000681.1:g.11350488C>T GRCh37
NC_000019.8:g.11211488C>T NCBI36
NG_031953.1:g.27681G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000587656.6:c.1644-1508G>A (DOCK6) ENSP00000468638.2:n.1644-1508G>A
ENST00000294618.12:c.1644-1508G>A (DOCK6) MANE Select ENSP00000294618.6:n.1644-1508G>A
ENST00000252453.12:c.175C>T (ANGPTL8) MANE Select ENSP00000252453.7:p.Arg59Trp
ENST00000294618.11:c.1644-1508G>A (DOCK6) ENSP00000294618.6:n.1644-1508G>A
ENST00000591200.5:c.1-323C>T (ANGPTL8) ENSP00000464941.1:n.1-323C>T
ENST00000616433.4:c.175C>T (ANGPTL8) ENSP00000479969.1:p.Arg59Trp
NM_018687.6:c.175C>T (ANGPTL8) NP_061157.3:p.Arg59Trp
NM_020812.3:c.1644-1508G>A (DOCK6) NP_065863.2:n.1644-1508G>A
XM_005260000.2:c.1644-1508G>A (DOCK6) XP_005260057.1:n.1644-1508G>A
XM_005260001.2:c.1644-1508G>A (DOCK6) XP_005260058.1:n.1644-1508G>A
XM_011528150.1:c.1677-1508G>A (DOCK6) XP_011526452.1:n.1677-1508G>A
XM_011528151.1:c.1677-1508G>A (DOCK6) XP_011526453.1:n.1677-1508G>A
XM_011528152.1:c.1677-1508G>A (DOCK6) XP_011526454.1:n.1677-1508G>A
XM_011528153.1:c.1677-1508G>A (DOCK6) XP_011526455.1:n.1677-1508G>A
XR_936195.1:n.1738-1508G>A (DOCK6)
XR_936196.1:n.1738-1508G>A (DOCK6)
XR_936197.1:n.1738-1508G>A (DOCK6)
XR_936198.1:n.1738-1508G>A (DOCK6)
NM_001367830.1:c.1644-1508G>A (DOCK6) NP_001354759.1:n.1644-1508G>A
NM_018687.7:c.175C>T (ANGPTL8) MANE Select NP_061157.3:p.Arg59Trp
NM_020812.4:c.1644-1508G>A (DOCK6) MANE Select NP_065863.2:n.1644-1508G>A
Search 100 bp 5'
Search 100 bp 3'