HGVS | Genome Assembly |
---|---|
NC_000020.11:g.1994123G>A , CM000682.2:g.1994123G>A | GRCh38 |
NC_000020.10:g.1974769G>A , CM000682.1:g.1974769G>A | GRCh37 |
NC_000020.9:g.1922769G>A | NCBI36 |
NG_028027.1:g.5123C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651882.1:c.-289C>T (PDYN) | ENSP00000498752.1:n.-289C>T | |
ENST00000539905.5:c.-232C>T (PDYN) | ENSP00000440185.1:n.-232C>T | |
NM_001190898.2:c.-289C>T (PDYN) | NP_001177827.1:n.-289C>T | |
NM_001190899.2:c.-232C>T (PDYN) | NP_001177828.1:n.-232C>T | |
NM_024411.4:c.-292C>T (PDYN) | NP_077722.1:n.-292C>T | |
XR_244229.1:n.1217-12809G>A (PDYN-AS1) | ||
NR_134520.1:n.1253-12809G>A (PDYN-AS1) |