HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52492684T>A , CM000674.2:g.52492684T>A | GRCh38 |
NC_000012.11:g.52886468T>A , CM000674.1:g.52886468T>A | GRCh37 |
NC_000012.10:g.51172735T>A | NCBI36 |
NG_008298.1:g.5714A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.505A>T MANE Select | ENSP00000369317.3:p.Thr169Ser | |
ENST00000330722.6:c.505A>T | ENSP00000369317.3:p.Thr169Ser | |
ENST00000549898.5:n.26A>T | ||
NM_005554.3:c.505A>T | NP_005545.1:p.Thr169Ser | |
NM_005554.4:c.505A>T MANE Select | NP_005545.1:p.Thr169Ser |