HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766031T>A , CM000674.2:g.57766031T>A | GRCh38 |
NC_000012.11:g.58159814T>A , CM000674.1:g.58159814T>A | GRCh37 |
NC_000012.10:g.56446081T>A | NCBI36 |
NG_007076.1:g.6163A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000546609.2:n.274A>T | ||
ENST00000713544.1:c.362A>T | ENSP00000518840.1:p.Gln121Leu | |
ENST00000713545.1:c.362A>T | ENSP00000518841.1:p.Gln121Leu | |
ENST00000228606.9:c.362A>T MANE Select | ENSP00000228606.4:p.Gln121Leu | |
ENST00000228606.8:c.362A>T | ENSP00000228606.4:p.Gln121Leu | |
ENST00000546496.1:n.190A>T | ||
ENST00000546609.1:c.274A>T | ||
ENST00000547344.5:n.416A>T | ||
ENST00000552186.1:n.481A>T | ||
NM_000785.3:c.362A>T | NP_000776.1:p.Gln121Leu | |
NM_000785.4:c.362A>T MANE Select | NP_000776.1:p.Gln121Leu |