Canonical Allele Identifier: CA2020587172
Gene: PDE3A HGNC NCBI

Linked Data

dbSNP Id: rs1565526018
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20368750G>A , CM000674.2:g.20368750G>A GRCh38
NC_000012.11:g.20521684G>A , CM000674.1:g.20521684G>A GRCh37
NC_000012.10:g.20412951G>A NCBI36
NG_030033.1:g.4506G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000359062.4:c.-535G>A MANE Select ENSP00000351957.3:n.-535G>A
XM_006719086.2:c.-535G>A XP_006719149.2:n.-535G>A
NM_000921.5:c.-535G>A MANE Select NP_000912.3:n.-535G>A
NM_001378407.1:c.-535G>A NP_001365336.1:n.-535G>A
NM_001378408.1:c.-1563G>A NP_001365337.1:n.-1563G>A
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