HGVS | Genome Assembly |
---|---|
NC_000023.11:g.136658942T= , CM000685.2:g.136658942T= | GRCh38 |
NC_000023.10:g.135741101T= , CM000685.1:g.135741101T= | GRCh37 |
NC_000023.9:g.135568767T= | NCBI36 |
NG_007280.1:g.15766T= , LRG_141:g.15766T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695724.1:c.*28-97T= | ENSP00000512122.1:n.*28-97T= | |
ENST00000695725.1:c.157-97T= | ENSP00000512123.1:n.157-97T= | |
ENST00000695726.1:n.2378-97T= | ||
ENST00000695729.1:n.3213-97T= | ||
ENST00000370629.7:c.410-97T= MANE Select | ENSP00000359663.2:n.410-97T= | |
ENST00000370628.2:c.347-97T= | ENSP00000359662.2:n.347-97T= | |
ENST00000370629.6:c.410-97T= | ENSP00000359663.2:n.410-97T= | |
NM_000074.2:c.410-97T= , LRG_141t1:c.410-97T= | NP_000065.1:n.410-97T= | |
NM_000074.3:c.410-97T= MANE Select | NP_000065.1:n.410-97T= |