Canonical Allele Identifier: CA573721962
Gene: PDE1C HGNC NCBI

Linked Data

dbSNP Id: rs1339960008
gnomAD v2: 7-32376683-C-G
gnomAD v3: 7-32337071-C-G
gnomAD v4: 7-32337071-C-G
MyVariant Identifiers: chr7:g.32376683C>G (hg19) chr7:g.32337071C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.32337071C>G , CM000669.2:g.32337071C>G GRCh38
NC_000007.13:g.32376683C>G , CM000669.1:g.32376683C>G GRCh37
NC_000007.12:g.32343208C>G NCBI36
NG_051183.1:g.96154G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000672256.1:c.310+90751G>C ENSP00000499831.1:n.310+90751G>C
NM_001322059.1:c.310+90751G>C NP_001308988.1:n.310+90751G>C
NM_001322059.2:c.310+90751G>C NP_001308988.1:n.310+90751G>C
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