HGVS | Genome Assembly |
---|---|
NC_000020.11:g.1994129A>T , CM000682.2:g.1994129A>T | GRCh38 |
NC_000020.10:g.1974775A>T , CM000682.1:g.1974775A>T | GRCh37 |
NC_000020.9:g.1922775A>T | NCBI36 |
NG_028027.1:g.5117T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651882.1:c.-295T>A (PDYN) | ENSP00000498752.1:n.-295T>A | |
ENST00000539905.5:c.-238T>A (PDYN) | ENSP00000440185.1:n.-238T>A | |
NM_001190898.2:c.-295T>A (PDYN) | NP_001177827.1:n.-295T>A | |
NM_001190899.2:c.-238T>A (PDYN) | NP_001177828.1:n.-238T>A | |
NM_024411.4:c.-298T>A (PDYN) | NP_077722.1:n.-298T>A | |
XR_244229.1:n.1217-12803A>T (PDYN-AS1) | ||
NR_134520.1:n.1253-12803A>T (PDYN-AS1) |