Canonical Allele Identifier: CA686318113
Gene: PDE3A HGNC NCBI

Linked Data

dbSNP Id: rs1207689552
gnomAD v3: 12-20368789-G-A
gnomAD v4: 12-20368789-G-A
MyVariant Identifiers: chr12:g.20521723G>A (hg19) chr12:g.20368789G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20368789G>A , CM000674.2:g.20368789G>A GRCh38
NC_000012.11:g.20521723G>A , CM000674.1:g.20521723G>A GRCh37
NC_000012.10:g.20412990G>A NCBI36
NG_030033.1:g.4545G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359062.4:c.-496G>A MANE Select ENSP00000351957.3:n.-496G>A
XM_006719086.2:c.-496G>A XP_006719149.2:n.-496G>A
NM_000921.5:c.-496G>A MANE Select NP_000912.3:n.-496G>A
NM_001378407.1:c.-496G>A NP_001365336.1:n.-496G>A
NM_001378408.1:c.-1524G>A NP_001365337.1:n.-1524G>A
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