HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189563619C>A , CM000664.2:g.189563619C>A | GRCh38 |
NC_000002.11:g.190428345C>A , CM000664.1:g.190428345C>A | GRCh37 |
NC_000002.10:g.190136590C>A | NCBI36 |
NG_009027.1:g.22193G>T , LRG_837:g.22193G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261024.7:c.1367G>T MANE Select | ENSP00000261024.3:p.Ser456Ile | |
ENST00000261024.6:c.1367G>T | ENSP00000261024.2:p.Ser456Ile | |
NM_014585.5:c.1367G>T , LRG_837t1:c.1367G>T | NP_055400.1:p.Ser456Ile | |
XM_005246505.1:c.1247G>T | XP_005246562.1:p.Ser416Ile | |
XM_005246505.2:c.1247G>T | XP_005246562.1:p.Ser416Ile | |
XM_017003938.2:c.1247G>T | XP_016859427.1:p.Ser416Ile | |
NM_014585.6:c.1367G>T MANE Select | NP_055400.1:p.Ser456Ile |