HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57766140T>C , CM000674.2:g.57766140T>C | GRCh38 |
NC_000012.11:g.58159923T>C , CM000674.1:g.58159923T>C | GRCh37 |
NC_000012.10:g.56446190T>C | NCBI36 |
NG_007076.1:g.6054A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546609.2:n.165A>G | ||
ENST00000713544.1:c.253A>G | ENSP00000518840.1:p.Thr85Ala | |
ENST00000713545.1:c.253A>G | ENSP00000518841.1:p.Thr85Ala | |
ENST00000228606.9:c.253A>G MANE Select | ENSP00000228606.4:p.Thr85Ala | |
ENST00000228606.8:c.253A>G | ENSP00000228606.4:p.Thr85Ala | |
ENST00000546496.1:n.81A>G | ||
ENST00000546609.1:c.165A>G | ||
ENST00000547344.5:n.307A>G | ||
ENST00000552186.1:n.372A>G | ||
NM_000785.3:c.253A>G | NP_000776.1:p.Thr85Ala | |
NM_000785.4:c.253A>G MANE Select | NP_000776.1:p.Thr85Ala |