HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160130480G= , CM000663.2:g.160130480G= | GRCh38 |
NC_000001.10:g.160100270G= , CM000663.1:g.160100270G= | GRCh37 |
NC_000001.9:g.158366894G= | NCBI36 |
NG_008014.1:g.19723G= , LRG_6:g.19723G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361216.8:c.1710G= MANE Select | ENSP00000354490.3:p.Thr570= | |
ENST00000361216.7:c.1710G= | ENSP00000354490.3:p.Thr570= | |
ENST00000392233.7:c.1710G= | ENSP00000376066.3:p.Thr570= | |
ENST00000447527.1:c.842G= | ||
ENST00000472488.5:n.1813G= | ||
NM_000702.3:c.1710G= | NP_000693.1:p.Thr570= | |
NM_000702.4:c.1710G= MANE Select | NP_000693.1:p.Thr570= |