HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586521T>G , CM000673.2:g.67586521T>G | GRCh38 |
NC_000011.9:g.67353992T>G , CM000673.1:g.67353992T>G | GRCh37 |
NC_000011.8:g.67110568T>G | NCBI36 |
NG_012075.1:g.7927T>G , LRG_723:g.7927T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.469T>G | ENSP00000381604.1:p.Phe157Val | |
ENST00000398606.10:c.577T>G MANE Select | ENSP00000381607.3:p.Phe193Val | |
ENST00000398603.5:c.469T>G | ENSP00000381604.1:p.Phe157Val | |
ENST00000398606.7:c.577T>G | ENSP00000381607.3:p.Phe193Val | |
ENST00000467591.1:n.688T>G | ||
ENST00000494593.1:n.1549T>G | ||
ENST00000498765.5:c.640T>G | ||
NM_000852.3:c.577T>G , LRG_723t1:c.577T>G | NP_000843.1:p.Phe193Val | |
NM_000852.4:c.577T>G MANE Select | NP_000843.1:p.Phe193Val |