HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119402272C= , CM000665.2:g.119402272C= | GRCh38 |
NC_000003.11:g.119121119C= , CM000665.1:g.119121119C= | GRCh37 |
NC_000003.10:g.120603809C= | NCBI36 |
NG_007665.2:g.112900C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.1520C= MANE Select | ENSP00000264245.4:p.Thr507= | |
ENST00000264245.8:c.1520C= | ENSP00000264245.4:p.Thr507= | |
NM_020754.3:c.1520C= | NP_065805.2:p.Thr507= | |
XM_005247671.3:c.1427C= | XP_005247728.1:p.Thr476= | |
XM_006713714.2:c.1460C= | XP_006713777.1:p.Thr487= | |
XM_006713714.3:c.1460C= | XP_006713777.1:p.Thr487= | |
XM_017006955.1:c.1028C= | XP_016862444.1:p.Thr343= | |
NM_020754.4:c.1520C= MANE Select | NP_065805.2:p.Thr507= |