HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67754130T>A , CM000666.2:g.67754130T>A | GRCh38 |
NC_000004.11:g.68619848T>A , CM000666.1:g.68619848T>A | GRCh37 |
NC_000004.10:g.68302443T>A | NCBI36 |
NG_009293.1:g.6957A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.206A>T MANE Select | ENSP00000226413.5:p.Lys69Ile | |
ENST00000226413.4:c.206A>T | ENSP00000226413.4:p.Lys69Ile | |
ENST00000420975.2:c.206A>T | ENSP00000397561.2:p.Lys69Ile | |
NM_000406.2:c.206A>T | NP_000397.1:p.Lys69Ile | |
NM_001012763.1:c.206A>T | NP_001012781.1:p.Lys69Ile | |
NM_000406.3:c.206A>T MANE Select | NP_000397.1:p.Lys69Ile | |
NM_001012763.2:c.206A>T | NP_001012781.1:p.Lys69Ile |