HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35850973T>A , CM000681.2:g.35850973T>A | GRCh38 |
NC_000019.9:g.36341875T>A , CM000681.1:g.36341875T>A | GRCh37 |
NC_000019.8:g.41033715T>A | NCBI36 |
NG_013356.2:g.23315A>T , LRG_693:g.23315A>T | |
NG_051206.1:g.4339T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000378910.10:c.514A>T MANE Select | ENSP00000368190.4:p.Thr172Ser | |
ENST00000353632.6:c.514A>T | ENSP00000343634.5:p.Thr172Ser | |
ENST00000378910.9:c.514A>T | ENSP00000368190.4:p.Thr172Ser | |
NM_004646.3:c.514A>T , LRG_693t1:c.514A>T | NP_004637.1:p.Thr172Ser | |
NM_004646.4:c.514A>T MANE Select | NP_004637.1:p.Thr172Ser |