HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766132G= , CM000674.2:g.57766132G= | GRCh38 |
NC_000012.11:g.58159915G= , CM000674.1:g.58159915G= | GRCh37 |
NC_000012.10:g.56446182G= | NCBI36 |
NG_007076.1:g.6062C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546609.2:n.173C= | ||
ENST00000713544.1:c.261C= | ENSP00000518840.1:p.Tyr87= | |
ENST00000713545.1:c.261C= | ENSP00000518841.1:p.Tyr87= | |
ENST00000228606.9:c.261C= MANE Select | ENSP00000228606.4:p.Tyr87= | |
ENST00000228606.8:c.261C= | ENSP00000228606.4:p.Tyr87= | |
ENST00000546496.1:n.89C= | ||
ENST00000546609.1:c.173C= | ||
ENST00000547344.5:n.315C= | ||
ENST00000552186.1:n.380C= | ||
NM_000785.3:c.261C= | NP_000776.1:p.Tyr87= | |
NM_000785.4:c.261C= MANE Select | NP_000776.1:p.Tyr87= |