HGVS | Genome Assembly |
---|---|
NC_000003.12:g.191357205T= , CM000665.2:g.191357205T= | GRCh38 |
NC_000003.11:g.191074994T= , CM000665.1:g.191074994T= | GRCh37 |
NC_000003.10:g.192557688T= | NCBI36 |
NG_008994.1:g.33121T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000392455.9:c.112+55T= MANE Select | ENSP00000376249.4:n.112+55T= | |
ENST00000392456.4:c.112+55T= | ENSP00000376250.4:n.112+55T= | |
ENST00000392455.7:c.112+55T= | ENSP00000376249.3:n.112+55T= | |
ENST00000392456.3:c.112+55T= | ENSP00000376250.3:n.112+55T= | |
NM_174908.3:c.112+55T= | NP_777568.1:n.112+55T= | |
NM_178335.2:c.112+55T= | NP_848018.1:n.112+55T= | |
XM_011512460.1:c.112+55T= | XP_011510762.1:n.112+55T= | |
NM_178335.3:c.112+55T= MANE Select | NP_848018.1:n.112+55T= | |
NM_174908.4:c.112+55T= | NP_777568.1:n.112+55T= |