HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21854360G>T , CM000669.2:g.21854360G>T | GRCh38 |
NC_000007.13:g.21893978G>T , CM000669.1:g.21893978G>T | GRCh37 |
NC_000007.12:g.21860503G>T | NCBI36 |
NG_012886.2:g.316146G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.11107G>T MANE Select | ENSP00000475939.1:p.Glu3703Ter | |
ENST00000328843.10:c.11128G>T | ENSP00000330671.7:p.Glu3710Ter | |
ENST00000409508.7:c.11107G>T | ENSP00000475939.1:p.Glu3703Ter | |
ENST00000421290.1:n.290G>T | ||
ENST00000607413.5:n.370G>T | ||
ENST00000620169.4:c.11128G>T | ENSP00000481693.1:p.Glu3710Ter | |
NM_001277115.1:c.11107G>T | NP_001264044.1:p.Glu3703Ter | |
NM_001277115.2:c.11107G>T MANE Select | NP_001264044.1:p.Glu3703Ter |