HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766133T>A , CM000674.2:g.57766133T>A | GRCh38 |
NC_000012.11:g.58159916T>A , CM000674.1:g.58159916T>A | GRCh37 |
NC_000012.10:g.56446183T>A | NCBI36 |
NG_007076.1:g.6061A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000546609.2:n.172A>T | ||
ENST00000713544.1:c.260A>T | ENSP00000518840.1:p.Tyr87Phe | |
ENST00000713545.1:c.260A>T | ENSP00000518841.1:p.Tyr87Phe | |
ENST00000228606.9:c.260A>T MANE Select | ENSP00000228606.4:p.Tyr87Phe | |
ENST00000228606.8:c.260A>T | ENSP00000228606.4:p.Tyr87Phe | |
ENST00000546496.1:n.88A>T | ||
ENST00000546609.1:c.172A>T | ||
ENST00000547344.5:n.314A>T | ||
ENST00000552186.1:n.379A>T | ||
NM_000785.3:c.260A>T | NP_000776.1:p.Tyr87Phe | |
NM_000785.4:c.260A>T MANE Select | NP_000776.1:p.Tyr87Phe |