HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154503T>A , CM000681.2:g.55154503T>A | GRCh38 |
NC_000019.9:g.55665871T>A , CM000681.1:g.55665871T>A | GRCh37 |
NC_000019.8:g.60357683T>A | NCBI36 |
NG_007866.2:g.8230A>T , LRG_432:g.8230A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.372+238A>T MANE Select | ENSP00000341838.5:n.372+238A>T | |
ENST00000665070.1:c.405+205A>T | ENSP00000499482.1:n.405+205A>T | |
ENST00000344887.9:c.372+238A>T | ENSP00000341838.5:n.372+238A>T | |
ENST00000585806.5:n.371+238A>T | ||
ENST00000586669.5:n.380+238A>T | ||
ENST00000587176.5:n.794A>T | ||
ENST00000588882.1:c.297+238A>T | ENSP00000466729.1:n.297+238A>T | |
NM_000363.4:c.372+238A>T , LRG_432t1:c.372+238A>T | NP_000354.4:n.372+238A>T | |
NM_000363.5:c.372+238A>T MANE Select | NP_000354.4:n.372+238A>T |