HGVS | Genome Assembly |
---|---|
NC_000020.11:g.1994146T>C , CM000682.2:g.1994146T>C | GRCh38 |
NC_000020.10:g.1974792T>C , CM000682.1:g.1974792T>C | GRCh37 |
NC_000020.9:g.1922792T>C | NCBI36 |
NG_028027.1:g.5100A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651882.1:c.-312A>G (PDYN) | ENSP00000498752.1:n.-312A>G | |
ENST00000539905.5:c.-255A>G (PDYN) | ENSP00000440185.1:n.-255A>G | |
NM_001190898.2:c.-312A>G (PDYN) | NP_001177827.1:n.-312A>G | |
NM_001190899.2:c.-255A>G (PDYN) | NP_001177828.1:n.-255A>G | |
NM_024411.4:c.-315A>G (PDYN) | NP_077722.1:n.-315A>G | |
XR_244229.1:n.1217-12786T>C (PDYN-AS1) | ||
NR_134520.1:n.1253-12786T>C (PDYN-AS1) |