HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740622G= , CM000666.2:g.67740622G= | GRCh38 |
NC_000004.11:g.68606340G= , CM000666.1:g.68606340G= | GRCh37 |
NC_000004.10:g.68288935G= | NCBI36 |
NG_009293.1:g.20465C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.845C= MANE Select | ENSP00000226413.5:p.Pro282= | |
ENST00000226413.4:c.845C= | ENSP00000226413.4:p.Pro282= | |
ENST00000420975.2:c.717C= | ENSP00000397561.2:p.Ser239= | |
NM_000406.2:c.845C= | NP_000397.1:p.Pro282= | |
NM_001012763.1:c.717C= | NP_001012781.1:p.Ser239= | |
NM_000406.3:c.845C= MANE Select | NP_000397.1:p.Pro282= | |
NM_001012763.2:c.717C= | NP_001012781.1:p.Ser239= |