Canonical Allele Identifier: CA837670817
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs542442970
MyVariant Identifiers: chr7:g.32376671T>A (hg19) chr7:g.32337059T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32337059T>A , CM000669.2:g.32337059T>A GRCh38
NC_000007.13:g.32376671T>A , CM000669.1:g.32376671T>A GRCh37
NC_000007.12:g.32343196T>A NCBI36
NG_051183.1:g.96166A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+90763A>T ENSP00000499831.1:n.310+90763A>T
NM_001322059.1:c.310+90763A>T NP_001308988.1:n.310+90763A>T
NM_001322059.2:c.310+90763A>T NP_001308988.1:n.310+90763A>T
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