HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787113T>G , CM000686.2:g.2787113T>G | GRCh38 |
NC_000024.9:g.2655154T>G , CM000686.1:g.2655154T>G | GRCh37 |
NC_000024.8:g.2715154T>G | NCBI36 |
NG_011751.1:g.5639A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000679518.1:n.106+12374T>G | ||
ENST00000679825.1:n.225T>G | ||
ENST00000680285.1:n.320-2636T>G | ||
ENST00000680845.1:n.165+60T>G | ||
ENST00000681787.1:n.106+12374T>G | ||
ENST00000681940.1:n.106+12374T>G | ||
ENST00000383070.2:c.491A>C MANE Select | ENSP00000372547.1:p.Tyr164Ser | |
ENST00000383070.1:c.491A>C | ENSP00000372547.1:p.Tyr164Ser | |
NM_003140.2:c.491A>C | NP_003131.1:p.Tyr164Ser | |
NM_003140.3:c.491A>C MANE Select | NP_003131.1:p.Tyr164Ser |