HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1416114T>A , CM000667.2:g.1416114T>A | GRCh38 |
NC_000005.9:g.1416229T>A , CM000667.1:g.1416229T>A | GRCh37 |
NC_000005.8:g.1469229T>A | NCBI36 |
NG_015885.1:g.34315A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1015A>T MANE Select | ENSP00000270349.9:p.Thr339Ser | |
ENST00000270349.11:c.1015A>T | ENSP00000270349.9:p.Thr339Ser | |
ENST00000511750.1:n.465A>T | ||
NM_001044.4:c.1015A>T | NP_001035.1:p.Thr339Ser | |
NM_001044.5:c.1015A>T MANE Select | NP_001035.1:p.Thr339Ser |