Canonical Allele Identifier: CA2714202935
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs1785015939

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32404662A>T , CM000669.2:g.32404662A>T GRCh38
NC_000007.13:g.32444274A>T , CM000669.1:g.32444274A>T GRCh37
NC_000007.12:g.32410799A>T NCBI36
NG_051183.1:g.28563T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+23160T>A ENSP00000499831.1:n.310+23160T>A
NM_001322059.1:c.310+23160T>A NP_001308988.1:n.310+23160T>A
NM_001322059.2:c.310+23160T>A NP_001308988.1:n.310+23160T>A