Canonical Allele Identifier: CA1099956465
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs1783640866
gnomAD v3: 7-32337084-A-T
gnomAD v4: 7-32337084-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32337084A>T , CM000669.2:g.32337084A>T GRCh38
NC_000007.13:g.32376696A>T , CM000669.1:g.32376696A>T GRCh37
NC_000007.12:g.32343221A>T NCBI36
NG_051183.1:g.96141T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000672256.1:c.310+90738T>A ENSP00000499831.1:n.310+90738T>A
NM_001322059.1:c.310+90738T>A NP_001308988.1:n.310+90738T>A
NM_001322059.2:c.310+90738T>A NP_001308988.1:n.310+90738T>A