Canonical Allele Identifier: CA156183837
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs921836721
gnomAD v2: 7-32444449-A-C
gnomAD v3: 7-32404837-A-C
gnomAD v4: 7-32404837-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32404837A>C , CM000669.2:g.32404837A>C GRCh38
NC_000007.13:g.32444449A>C , CM000669.1:g.32444449A>C GRCh37
NC_000007.12:g.32410974A>C NCBI36
NG_051183.1:g.28388T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+22985T>G ENSP00000499831.1:n.310+22985T>G
NM_001322059.1:c.310+22985T>G NP_001308988.1:n.310+22985T>G
NM_001322059.2:c.310+22985T>G NP_001308988.1:n.310+22985T>G