HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625612T>A , CM000673.2:g.22625612T>A | GRCh38 |
NC_000011.9:g.22647158T>A , CM000673.1:g.22647158T>A | GRCh37 |
NC_000011.8:g.22603734T>A | NCBI36 |
NG_007425.1:g.5230A>T , LRG_527:g.5230A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.199A>T (FANCF) MANE Select | ENSP00000330875.3:p.Arg67Trp | |
ENST00000648096.1:n.104T>A (GAS2) | ||
ENST00000327470.4:c.199A>T (FANCF) | ENSP00000330875.3:p.Arg67Trp | |
NM_022725.3:c.199A>T , LRG_527t1:c.199A>T (FANCF) | NP_073562.1:p.Arg67Trp | |
NM_022725.4:c.199A>T (FANCF) MANE Select | NP_073562.1:p.Arg67Trp |