HGVS | Genome Assembly |
---|---|
NC_000011.10:g.65868562G>C , CM000673.2:g.65868562G>C | GRCh38 |
NC_000011.9:g.65636033G>C , CM000673.1:g.65636033G>C | GRCh37 |
NC_000011.8:g.65392609G>C | NCBI36 |
NG_012304.2:g.9373C>G | |
NG_053116.1:g.13501G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307998.11:c.795C>G MANE Select | ENSP00000309953.6:p.Phe265Leu | |
ENST00000307998.10:c.795C>G | ENSP00000309953.6:p.Phe265Leu | |
ENST00000526628.5:n.1361C>G | ||
ENST00000527969.1:n.1480C>G | ||
ENST00000528176.5:c.795C>G | ENSP00000434151.1:p.Phe265Leu | |
ENST00000531005.5:n.1789C>G | ||
ENST00000531972.5:c.795C>G | ENSP00000435295.1:p.Phe265Leu | |
ENST00000532084.5:n.221C>G | ||
NM_016938.4:c.795C>G | NP_058634.4:p.Phe265Leu | |
NR_037718.1:n.1054C>G | ||
NM_016938.5:c.795C>G MANE Select | NP_058634.4:p.Phe265Leu | |
NR_037718.2:n.920C>G |