HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99851545C>T , CM000672.2:g.99851545C>T | GRCh38 |
NC_000010.10:g.101611302C>T , CM000672.1:g.101611302C>T | GRCh37 |
NC_000010.9:g.101601292C>T | NCBI36 |
NG_011798.1:g.73840C>T | |
NG_011798.2:g.73948C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647814.1:c.4552C>T MANE Select | ENSP00000497274.1:p.Pro1518Ser | |
ENST00000648523.1:c.622C>T | ||
ENST00000370449.8:c.4552C>T | ENSP00000359478.4:p.Pro1518Ser | |
NM_000392.4:c.4552C>T | NP_000383.1:p.Pro1518Ser | |
XM_006717630.2:c.3856C>T | XP_006717693.1:p.Pro1286Ser | |
NM_000392.5:c.4552C>T MANE Select | NP_000383.2:p.Pro1518Ser | |
XM_006717630.3:c.3856C>T | XP_006717693.1:p.Pro1286Ser |