Canonical Allele Identifier: CA156183843

Gene: PDE1C

Linked Data

• dbSNP Id: rs913250638
• gnomAD v3: 7-32404853-G-C
• gnomAD v4: 7-32404853-G-C
• MyVariant Identifiers: chr7:g.32444465G>C (hg19) ; chr7:g.32404853G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.32404853G>C , CM000669.2:g.32404853G>C	GRCh38
NC_000007.13:g.32444465G>C , CM000669.1:g.32444465G>C	GRCh37
NC_000007.12:g.32410990G>C	NCBI36
NG_051183.1:g.28372C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000672256.1:c.310+22969C>G	ENSP00000499831.1:n.310+22969C>G
NM_001322059.1:c.310+22969C>G	NP_001308988.1:n.310+22969C>G
NM_001322059.2:c.310+22969C>G	NP_001308988.1:n.310+22969C>G