HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625378T>A , CM000673.2:g.22625378T>A | GRCh38 |
NC_000011.9:g.22646924T>A , CM000673.1:g.22646924T>A | GRCh37 |
NC_000011.8:g.22603500T>A | NCBI36 |
NG_007425.1:g.5464A>T , LRG_527:g.5464A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.433A>T MANE Select | ENSP00000330875.3:p.Met145Leu | |
ENST00000327470.4:c.433A>T | ENSP00000330875.3:p.Met145Leu | |
NM_022725.3:c.433A>T , LRG_527t1:c.433A>T | NP_073562.1:p.Met145Leu | |
NM_022725.4:c.433A>T MANE Select | NP_073562.1:p.Met145Leu |