HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18786104C>T , CM000681.2:g.18786104C>T | GRCh38 |
NC_000019.9:g.18896914C>T , CM000681.1:g.18896914C>T | GRCh37 |
NC_000019.8:g.18757914C>T | NCBI36 |
NG_007070.1:g.10201G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000222271.7:c.1350G>A MANE Select | ENSP00000222271.2:p.Thr450= | |
ENST00000222271.6:c.1350G>A | ENSP00000222271.2:p.Thr450= | |
ENST00000425807.1:c.1191G>A | ENSP00000403792.1:p.Thr397= | |
ENST00000542601.6:c.1251G>A | ENSP00000439156.2:p.Thr417= | |
NM_000095.2:c.1350G>A | NP_000086.2:p.Thr450= | |
NM_000095.3:c.1350G>A MANE Select | NP_000086.2:p.Thr450= |