HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766134A>C , CM000674.2:g.57766134A>C | GRCh38 |
NC_000012.11:g.58159917A>C , CM000674.1:g.58159917A>C | GRCh37 |
NC_000012.10:g.56446184A>C | NCBI36 |
NG_007076.1:g.6060T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000546609.2:n.171T>G | ||
ENST00000713544.1:c.259T>G | ENSP00000518840.1:p.Tyr87Asp | |
ENST00000713545.1:c.259T>G | ENSP00000518841.1:p.Tyr87Asp | |
ENST00000228606.9:c.259T>G MANE Select | ENSP00000228606.4:p.Tyr87Asp | |
ENST00000228606.8:c.259T>G | ENSP00000228606.4:p.Tyr87Asp | |
ENST00000546496.1:n.87T>G | ||
ENST00000546609.1:c.171T>G | ||
ENST00000547344.5:n.313T>G | ||
ENST00000552186.1:n.378T>G | ||
NM_000785.3:c.259T>G | NP_000776.1:p.Tyr87Asp | |
NM_000785.4:c.259T>G MANE Select | NP_000776.1:p.Tyr87Asp |