Canonical Allele Identifier: CA741913843
Gene: PDYN HGNC NCBI
PDYN-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1293511692
gnomAD v3: 20-1994147-G-T
gnomAD v4: 20-1994147-G-T
MyVariant Identifiers: chr20:g.1974793G>T (hg19) chr20:g.1994147G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.1994147G>T , CM000682.2:g.1994147G>T GRCh38
NC_000020.10:g.1974793G>T , CM000682.1:g.1974793G>T GRCh37
NC_000020.9:g.1922793G>T NCBI36
NG_028027.1:g.5099C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651882.1:c.-313C>A (PDYN) ENSP00000498752.1:n.-313C>A
ENST00000539905.5:c.-256C>A (PDYN) ENSP00000440185.1:n.-256C>A
NM_001190898.2:c.-313C>A (PDYN) NP_001177827.1:n.-313C>A
NM_001190899.2:c.-256C>A (PDYN) NP_001177828.1:n.-256C>A
NM_024411.4:c.-316C>A (PDYN) NP_077722.1:n.-316C>A
XR_244229.1:n.1217-12785G>T (PDYN-AS1)
NR_134520.1:n.1253-12785G>T (PDYN-AS1)
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