Canonical Allele Identifier: CA837670939
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs1239026321
gnomAD v3: 7-32337145-A-G
gnomAD v4: 7-32337145-A-G
MyVariant Identifiers: chr7:g.32376757A>G (hg19) chr7:g.32337145A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32337145A>G , CM000669.2:g.32337145A>G GRCh38
NC_000007.13:g.32376757A>G , CM000669.1:g.32376757A>G GRCh37
NC_000007.12:g.32343282A>G NCBI36
NG_051183.1:g.96080T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+90677T>C ENSP00000499831.1:n.310+90677T>C
NM_001322059.1:c.310+90677T>C NP_001308988.1:n.310+90677T>C
NM_001322059.2:c.310+90677T>C NP_001308988.1:n.310+90677T>C
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