HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38396465G>C , CM000671.2:g.38396465G>C | GRCh38 |
NC_000009.11:g.38396462G>C , CM000671.1:g.38396462G>C | GRCh37 |
NC_000009.10:g.38386462G>C | NCBI36 |
NG_012253.1:g.8761G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377698.4:c.717G>C MANE Select | ENSP00000366927.3:p.Thr239= | |
ENST00000377698.3:c.717G>C | ENSP00000366927.3:p.Thr239= | |
NM_000692.4:c.717G>C | NP_000683.3:p.Thr239= | |
XM_011517802.1:c.717G>C | XP_011516104.1:p.Thr239= | |
XM_011517802.2:c.717G>C | XP_011516104.1:p.Thr239= | |
NM_000692.5:c.717G>C MANE Select | NP_000683.3:p.Thr239= |