HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787017T>C , CM000686.2:g.2787017T>C | GRCh38 |
NC_000024.9:g.2655058T>C , CM000686.1:g.2655058T>C | GRCh37 |
NC_000024.8:g.2715058T>C | NCBI36 |
NG_011751.1:g.5735A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679518.1:n.106+12278T>C | ||
ENST00000679825.1:n.129T>C | ||
ENST00000680285.1:n.320-2732T>C | ||
ENST00000680845.1:n.129T>C | ||
ENST00000681787.1:n.106+12278T>C | ||
ENST00000681940.1:n.106+12278T>C | ||
ENST00000383070.2:c.587A>G MANE Select | ENSP00000372547.1:p.Asp196Gly | |
ENST00000383070.1:c.587A>G | ENSP00000372547.1:p.Asp196Gly | |
NM_003140.2:c.587A>G | NP_003131.1:p.Asp196Gly | |
NM_003140.3:c.587A>G MANE Select | NP_003131.1:p.Asp196Gly |