HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128849380G= , CM000669.2:g.128849380G= | GRCh38 |
NC_000007.13:g.128489434G= , CM000669.1:g.128489434G= | GRCh37 |
NC_000007.12:g.128276670G= | NCBI36 |
NG_011807.1:g.23952G= , LRG_870:g.23952G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000325888.13:c.5001G= MANE Select | ENSP00000327145.8:p.Thr1667= | |
ENST00000325888.12:c.5001G= | ENSP00000327145.8:p.Thr1667= | |
ENST00000346177.6:c.5001G= | ENSP00000344002.6:p.Thr1667= | |
NM_001127487.1:c.5001G= | NP_001120959.1:p.Thr1667= | |
NM_001458.4:c.5001G= , LRG_870t1:c.5001G= | NP_001449.3:p.Thr1667= | |
NM_001127487.2:c.5001G= | NP_001120959.1:p.Thr1667= | |
NM_001458.5:c.5001G= MANE Select | NP_001449.3:p.Thr1667= |