HGVS | Genome Assembly |
---|---|
NC_000008.11:g.24952654A>T , CM000670.2:g.24952654A>T | GRCh38 |
NC_000008.10:g.24810167A>T , CM000670.1:g.24810167A>T | GRCh37 |
NC_000008.9:g.24866084A>T | NCBI36 |
NG_008492.1:g.8964T>A , LRG_259:g.8964T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000610854.2:c.*156T>A MANE Select | ENSP00000482169.2:n.*156T>A | |
ENST00000610854.1:c.*156T>A | ENSP00000482169.1:n.*156T>A | |
ENST00000619417.1:c.*653T>A | ENSP00000483690.1:n.*653T>A | |
NM_006158.4:c.*156T>A , LRG_259t1:c.*156T>A | NP_006149.2:n.*156T>A | |
NM_006158.5:c.*156T>A MANE Select | NP_006149.2:n.*156T>A |