Canonical Allele Identifier: CA751459976
Gene: ZDHHC8 HGNC NCBI

Linked Data

dbSNP Id: rs1340060319
gnomAD v3: 22-20139979-G-A
gnomAD v4: 22-20139979-G-A
MyVariant Identifiers: chr22:g.20127502G>A (hg19) chr22:g.20139979G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20139979G>A , CM000684.2:g.20139979G>A GRCh38
NC_000022.10:g.20127502G>A , CM000684.1:g.20127502G>A GRCh37
NC_000022.9:g.18507502G>A NCBI36
NG_021420.1:g.13139G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000334554.12:c.557+87G>A MANE Select ENSP00000334490.7:n.557+87G>A
ENST00000320602.11:c.384+344G>A ENSP00000317804.7:n.384+344G>A
ENST00000334554.11:c.557+87G>A ENSP00000334490.7:n.557+87G>A
ENST00000405930.3:c.557+87G>A ENSP00000384716.3:n.557+87G>A
ENST00000468112.5:n.58-638G>A
ENST00000469212.5:n.43G>A
NM_001185024.1:c.557+87G>A NP_001171953.1:n.557+87G>A
NM_013373.3:c.557+87G>A NP_037505.1:n.557+87G>A
XM_006724239.2:c.557+87G>A XP_006724302.1:n.557+87G>A
NM_001185024.2:c.557+87G>A NP_001171953.1:n.557+87G>A
NM_013373.4:c.557+87G>A MANE Select NP_037505.1:n.557+87G>A
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