Canonical Allele Identifier: CA156183822
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs79940490
gnomAD v2: 7-32444409-T-C
gnomAD v3: 7-32404797-T-C
gnomAD v4: 7-32404797-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32404797T>C , CM000669.2:g.32404797T>C GRCh38
NC_000007.13:g.32444409T>C , CM000669.1:g.32444409T>C GRCh37
NC_000007.12:g.32410934T>C NCBI36
NG_051183.1:g.28428A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+23025A>G ENSP00000499831.1:n.310+23025A>G
NM_001322059.1:c.310+23025A>G NP_001308988.1:n.310+23025A>G
NM_001322059.2:c.310+23025A>G NP_001308988.1:n.310+23025A>G