HGVS | Genome Assembly |
---|---|
NC_000003.12:g.8745780C>T , CM000665.2:g.8745780C>T | GRCh38 |
NC_000003.11:g.8787466C>T , CM000665.1:g.8787466C>T | GRCh37 |
NC_000003.10:g.8762466C>T | NCBI36 |
NG_008797.2:g.16971C>T , LRG_329:g.16971C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343849.3:c.369C>T MANE Select | ENSP00000341940.2:p.Leu123= | |
ENST00000343849.2:c.369C>T | ENSP00000341940.2:p.Leu123= | |
ENST00000397368.2:c.369C>T | ENSP00000380525.2:p.Leu123= | |
ENST00000472766.1:n.155+11790C>T | ||
NM_001234.4:c.369C>T | NP_001225.1:p.Leu123= | |
NM_033337.2:c.369C>T , LRG_329t1:c.369C>T | NP_203123.1:p.Leu123= | |
NM_001234.5:c.369C>T | NP_001225.1:p.Leu123= | |
NM_033337.3:c.369C>T MANE Select | NP_203123.1:p.Leu123= |