HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114484T>A , CM000667.2:g.140114484T>A | GRCh38 |
NC_000005.9:g.139494069T>A , CM000667.1:g.139494069T>A | GRCh37 |
NC_000005.8:g.139474253T>A | NCBI36 |
NG_041813.1:g.5362T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000331327.5:c.303T>A MANE Select | ENSP00000332706.3:p.Thr101= | |
ENST00000505703.2:c.303T>A | ENSP00000498560.1:p.Thr101= | |
ENST00000651386.1:c.303T>A | ENSP00000499133.1:p.Thr101= | |
ENST00000331327.4:c.303T>A | ENSP00000332706.3:p.Thr101= | |
NM_005859.4:c.303T>A | NP_005850.1:p.Thr101= | |
NM_005859.5:c.303T>A MANE Select | NP_005850.1:p.Thr101= |