HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339634G= , CM000669.2:g.17339634G= | GRCh38 |
NC_000007.13:g.17379258G= , CM000669.1:g.17379258G= | GRCh37 |
NC_000007.12:g.17345783G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242057.9:c.1809G= MANE Select | ENSP00000242057.4:p.Gln603= | |
ENST00000637807.1:c.1779G= | ENSP00000490530.1:p.Gln593= | |
ENST00000642825.1:c.1764G= | ENSP00000495987.1:p.Gln588= | |
ENST00000242057.8:c.1809G= | ENSP00000242057.4:p.Gln603= | |
ENST00000463496.1:c.1809G= | ENSP00000436466.1:p.Gln603= | |
NM_001621.4:c.1809G= | NP_001612.1:p.Gln603= | |
NM_001621.5:c.1809G= MANE Select | NP_001612.1:p.Gln603= |