HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625711C>G , CM000673.2:g.22625711C>G | GRCh38 |
NC_000011.9:g.22647257C>G , CM000673.1:g.22647257C>G | GRCh37 |
NC_000011.8:g.22603833C>G | NCBI36 |
NG_007425.1:g.5131G>C , LRG_527:g.5131G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.100G>C (FANCF) MANE Select | ENSP00000330875.3:p.Ala34Pro | |
ENST00000648096.1:n.203C>G (GAS2) | ||
ENST00000327470.4:c.100G>C (FANCF) | ENSP00000330875.3:p.Ala34Pro | |
ENST00000528582.5:c.-123C>G (GAS2) | ENSP00000432584.1:n.-123C>G | |
NM_022725.3:c.100G>C , LRG_527t1:c.100G>C (FANCF) | NP_073562.1:p.Ala34Pro | |
NM_022725.4:c.100G>C (FANCF) MANE Select | NP_073562.1:p.Ala34Pro |