HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44352141T>A , CM000679.2:g.44352141T>A | GRCh38 |
NC_000017.10:g.42429509T>A , CM000679.1:g.42429509T>A | GRCh37 |
NC_000017.9:g.39785035T>A | NCBI36 |
NG_007886.1:g.12019T>A , LRG_661:g.12019T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000053867.8:c.1306T>A MANE Select | ENSP00000053867.2:p.Leu436Ile | |
ENST00000639447.1:c.1137-388T>A | ENSP00000492014.1:n.1137-388T>A | |
ENST00000053867.7:c.1306T>A | ENSP00000053867.2:p.Leu436Ile | |
ENST00000586443.1:c.747T>A | ||
ENST00000589265.5:c.835T>A | ENSP00000467616.1:p.Leu279Ile | |
NM_002087.3:c.1306T>A | NP_002078.1:p.Leu436Ile | |
XM_005257253.1:c.1306T>A | XP_005257310.1:p.Leu436Ile | |
XM_024450730.1:c.1306T>A | XP_024306498.1:p.Leu436Ile | |
NM_002087.4:c.1306T>A MANE Select | NP_002078.1:p.Leu436Ile |