Canonical Allele Identifier: CA573721963
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs1398313023
gnomAD v2: 7-32376709-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32337097A>G , CM000669.2:g.32337097A>G GRCh38
NC_000007.13:g.32376709A>G , CM000669.1:g.32376709A>G GRCh37
NC_000007.12:g.32343234A>G NCBI36
NG_051183.1:g.96128T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+90725T>C ENSP00000499831.1:n.310+90725T>C
NM_001322059.1:c.310+90725T>C NP_001308988.1:n.310+90725T>C
NM_001322059.2:c.310+90725T>C NP_001308988.1:n.310+90725T>C