Canonical Allele Identifier: CA741913834
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1184656767
gnomAD v3: 20-1994116-C-T
gnomAD v4: 20-1994116-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994116C>T , CM000682.2:g.1994116C>T GRCh38
NC_000020.10:g.1974762C>T , CM000682.1:g.1974762C>T GRCh37
NC_000020.9:g.1922762C>T NCBI36
NG_028027.1:g.5130G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651882.1:c.-282G>A (PDYN) ENSP00000498752.1:n.-282G>A
ENST00000539905.5:c.-225G>A (PDYN) ENSP00000440185.1:n.-225G>A
NM_001190898.2:c.-282G>A (PDYN) NP_001177827.1:n.-282G>A
NM_001190899.2:c.-225G>A (PDYN) NP_001177828.1:n.-225G>A
NM_024411.4:c.-285G>A (PDYN) NP_077722.1:n.-285G>A
XR_244229.1:n.1217-12816C>T (PDYN-AS1)
NR_134520.1:n.1253-12816C>T (PDYN-AS1)