HGVS | Genome Assembly |
---|---|
NC_000017.11:g.58280366C>A , CM000679.2:g.58280366C>A | GRCh38 |
NC_000017.10:g.56357727C>A , CM000679.1:g.56357727C>A | GRCh37 |
NC_000017.9:g.53712726C>A | NCBI36 |
NG_009629.1:g.5570G>T , LRG_84:g.5570G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000225275.4:c.248G>T MANE Select | ENSP00000225275.3:p.Ser83Ile | |
ENST00000225275.3:c.248G>T | ENSP00000225275.3:p.Ser83Ile | |
ENST00000580005.1:n.177G>T | ||
NM_000250.1:c.248G>T , LRG_84t1:c.248G>T | NP_000241.1:p.Ser83Ile | |
XM_011524821.1:c.434G>T | XP_011523123.1:p.Ser145Ile | |
XM_011524822.1:c.-38+239G>T | XP_011523124.1:n.-38+239G>T | |
XM_011524823.1:c.434G>T | XP_011523125.1:p.Ser145Ile | |
NM_000250.2:c.248G>T MANE Select | NP_000241.1:p.Ser83Ile |