Canonical Allele Identifier: CA156183870
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs1010509405
gnomAD v3: 7-32404931-T-C
gnomAD v4: 7-32404931-T-C
MyVariant Identifiers: chr7:g.32444543T>C (hg19) chr7:g.32404931T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32404931T>C , CM000669.2:g.32404931T>C GRCh38
NC_000007.13:g.32444543T>C , CM000669.1:g.32444543T>C GRCh37
NC_000007.12:g.32411068T>C NCBI36
NG_051183.1:g.28294A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+22891A>G ENSP00000499831.1:n.310+22891A>G
NM_001322059.1:c.310+22891A>G NP_001308988.1:n.310+22891A>G
NM_001322059.2:c.310+22891A>G NP_001308988.1:n.310+22891A>G
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