HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94417797G= , CM000669.2:g.94417797G= | GRCh38 |
NC_000007.13:g.94047109G= , CM000669.1:g.94047109G= | GRCh37 |
NC_000007.12:g.93885045G= | NCBI36 |
NG_007405.1:g.28237G= , LRG_2:g.28237G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.1937G= MANE Select | ENSP00000297268.6:p.Gly646= | |
ENST00000297268.10:c.1937G= | ENSP00000297268.6:p.Gly646= | |
ENST00000461525.5:n.26G= | ||
ENST00000473573.5:n.274G= | ||
ENST00000497316.5:n.334G= | ||
ENST00000620463.1:c.1931G= | ENSP00000477719.1:p.Gly644= | |
NM_000089.3:c.1937G= , LRG_2t1:c.1937G= | NP_000080.2:p.Gly646= | |
NM_000089.4:c.1937G= MANE Select | NP_000080.2:p.Gly646= |