HGVS | Genome Assembly |
---|---|
NC_000024.10:g.2787414T>G , CM000686.2:g.2787414T>G | GRCh38 |
NC_000024.9:g.2655455T>G , CM000686.1:g.2655455T>G | GRCh37 |
NC_000024.8:g.2715455T>G | NCBI36 |
NG_011751.1:g.5338A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000679518.1:n.106+12675T>G | ||
ENST00000679825.1:n.526T>G | ||
ENST00000680285.1:n.320-2335T>G | ||
ENST00000680845.1:n.166-66T>G | ||
ENST00000681787.1:n.106+12675T>G | ||
ENST00000681940.1:n.106+12675T>G | ||
ENST00000383070.2:c.190A>C MANE Select | ENSP00000372547.1:p.Met64Leu | |
ENST00000383070.1:c.190A>C | ENSP00000372547.1:p.Met64Leu | |
NM_003140.2:c.190A>C | NP_003131.1:p.Met64Leu | |
NM_003140.3:c.190A>C MANE Select | NP_003131.1:p.Met64Leu |