Canonical Allele Identifier: CA741913840
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1253196075
gnomAD v3: 20-1994130-G-A
gnomAD v4: 20-1994130-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994130G>A , CM000682.2:g.1994130G>A GRCh38
NC_000020.10:g.1974776G>A , CM000682.1:g.1974776G>A GRCh37
NC_000020.9:g.1922776G>A NCBI36
NG_028027.1:g.5116C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000651882.1:c.-296C>T (PDYN) ENSP00000498752.1:n.-296C>T
ENST00000539905.5:c.-239C>T (PDYN) ENSP00000440185.1:n.-239C>T
NM_001190898.2:c.-296C>T (PDYN) NP_001177827.1:n.-296C>T
NM_001190899.2:c.-239C>T (PDYN) NP_001177828.1:n.-239C>T
NM_024411.4:c.-299C>T (PDYN) NP_077722.1:n.-299C>T
XR_244229.1:n.1217-12802G>A (PDYN-AS1)
NR_134520.1:n.1253-12802G>A (PDYN-AS1)