HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625509C= , CM000673.2:g.22625509C= | GRCh38 |
NC_000011.9:g.22647055C= , CM000673.1:g.22647055C= | GRCh37 |
NC_000011.8:g.22603631C= | NCBI36 |
NG_007425.1:g.5333G= , LRG_527:g.5333G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.302G= (FANCF) MANE Select | ENSP00000330875.3:p.Arg101= | |
ENST00000648096.1:n.1C= (GAS2) | ||
ENST00000327470.4:c.302G= (FANCF) | ENSP00000330875.3:p.Arg101= | |
NM_022725.3:c.302G= , LRG_527t1:c.302G= (FANCF) | NP_073562.1:p.Arg101= | |
NM_022725.4:c.302G= (FANCF) MANE Select | NP_073562.1:p.Arg101= |