HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160130575A>T , CM000663.2:g.160130575A>T | GRCh38 |
NC_000001.10:g.160100365A>T , CM000663.1:g.160100365A>T | GRCh37 |
NC_000001.9:g.158366989A>T | NCBI36 |
NG_008014.1:g.19818A>T , LRG_6:g.19818A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361216.8:c.1805A>T MANE Select | ENSP00000354490.3:p.Lys602Met | |
ENST00000361216.7:c.1805A>T | ENSP00000354490.3:p.Lys602Met | |
ENST00000392233.7:c.1805A>T | ENSP00000376066.3:p.Lys602Met | |
ENST00000447527.1:c.937A>T | ||
ENST00000472488.5:n.1908A>T | ||
NM_000702.3:c.1805A>T | NP_000693.1:p.Lys602Met | |
NM_000702.4:c.1805A>T MANE Select | NP_000693.1:p.Lys602Met |