Canonical Allele Identifier: CA686318100
Gene: PDE3A HGNC NCBI

Linked Data

dbSNP Id: rs1455929293
gnomAD v3: 12-20368753-G-T
gnomAD v4: 12-20368753-G-T
MyVariant Identifiers: chr12:g.20521687G>T (hg19) chr12:g.20368753G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.20368753G>T , CM000674.2:g.20368753G>T GRCh38
NC_000012.11:g.20521687G>T , CM000674.1:g.20521687G>T GRCh37
NC_000012.10:g.20412954G>T NCBI36
NG_030033.1:g.4509G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359062.4:c.-532G>T MANE Select ENSP00000351957.3:n.-532G>T
XM_006719086.2:c.-532G>T XP_006719149.2:n.-532G>T
NM_000921.5:c.-532G>T MANE Select NP_000912.3:n.-532G>T
NM_001378407.1:c.-532G>T NP_001365336.1:n.-532G>T
NM_001378408.1:c.-1560G>T NP_001365337.1:n.-1560G>T
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