Canonical Allele Identifier: CA156183813
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs369558429

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32404758C>T , CM000669.2:g.32404758C>T GRCh38
NC_000007.13:g.32444370C>T , CM000669.1:g.32444370C>T GRCh37
NC_000007.12:g.32410895C>T NCBI36
NG_051183.1:g.28467G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+23064G>A ENSP00000499831.1:n.310+23064G>A
NM_001322059.1:c.310+23064G>A NP_001308988.1:n.310+23064G>A
NM_001322059.2:c.310+23064G>A NP_001308988.1:n.310+23064G>A