HGVS | Genome Assembly |
---|---|
NC_000019.10:g.4816583T>C , CM000681.2:g.4816583T>C | GRCh38 |
NC_000019.9:g.4816595T>C , CM000681.1:g.4816595T>C | GRCh37 |
NC_000019.8:g.4767595T>C | NCBI36 |
NG_031998.1:g.20160A>G , LRG_358:g.20160A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248244.6:c.1795A>G MANE Select | ENSP00000248244.4:p.Thr599Ala | |
ENST00000248244.5:c.1795A>G | ENSP00000248244.4:p.Thr599Ala | |
ENST00000621756.1:c.1378A>G | ENSP00000479467.1:p.Thr460Ala | |
NM_182919.3:c.1795A>G , LRG_358t1:c.1795A>G | NP_891549.1:p.Thr599Ala | |
NM_001385678.1:c.1753A>G | NP_001372607.1:p.Thr585Ala | |
NM_001385679.1:c.1660A>G | NP_001372608.1:p.Thr554Ala | |
NM_001385680.1:c.1153A>G | NP_001372609.1:p.Thr385Ala | |
NM_182919.4:c.1795A>G MANE Select | NP_891549.1:p.Thr599Ala |