HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787547T>G , CM000681.2:g.18787547T>G | GRCh38 |
NC_000019.9:g.18898356T>G , CM000681.1:g.18898356T>G | GRCh37 |
NC_000019.8:g.18759356T>G | NCBI36 |
NG_007070.1:g.8759A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1079A>C MANE Select | ENSP00000222271.2:p.Lys360Thr | |
ENST00000222271.6:c.1079A>C | ENSP00000222271.2:p.Lys360Thr | |
ENST00000425807.1:c.920A>C | ENSP00000403792.1:p.Lys307Thr | |
ENST00000542601.6:c.980A>C | ENSP00000439156.2:p.Lys327Thr | |
NM_000095.2:c.1079A>C | NP_000086.2:p.Lys360Thr | |
NM_000095.3:c.1079A>C MANE Select | NP_000086.2:p.Lys360Thr |