HGVS | Genome Assembly |
---|---|
NC_000004.12:g.67740616T>G , CM000666.2:g.67740616T>G | GRCh38 |
NC_000004.11:g.68606334T>G , CM000666.1:g.68606334T>G | GRCh37 |
NC_000004.10:g.68288929T>G | NCBI36 |
NG_009293.1:g.20471A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000226413.5:c.851A>C MANE Select | ENSP00000226413.5:p.Tyr284Ser | |
ENST00000226413.4:c.851A>C | ENSP00000226413.4:p.Tyr284Ser | |
ENST00000420975.2:c.723A>C | ENSP00000397561.2:p.Leu241= | |
NM_000406.2:c.851A>C | NP_000397.1:p.Tyr284Ser | |
NM_001012763.1:c.723A>C | NP_001012781.1:p.Leu241= | |
NM_000406.3:c.851A>C MANE Select | NP_000397.1:p.Tyr284Ser | |
NM_001012763.2:c.723A>C | NP_001012781.1:p.Leu241= |