HGVS | Genome Assembly |
---|---|
NC_000019.10:g.58487906A>T , CM000681.2:g.58487906A>T | GRCh38 |
NC_000019.9:g.58999273A>T , CM000681.1:g.58999273A>T | GRCh37 |
NC_000019.8:g.63691085A>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000595851.5:c.*22-4260T>A (SLC27A5) | ENSP00000469512.1:n.*22-4260T>A | |
NM_001304453.1:c.803-1384A>T (ZNF446) | NP_001291382.1:n.803-1384A>T | |
XM_006723266.2:c.803-1384A>T (ZNF446) | XP_006723329.1:n.803-1384A>T | |
XM_006723266.4:c.803-1384A>T (ZNF446) | XP_006723329.1:n.803-1384A>T | |
XM_017026950.2:c.1005-1384A>T (ZNF446) | XP_016882439.1:n.1005-1384A>T |