HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94056620G>C , CM000663.2:g.94056620G>C | GRCh38 |
NC_000001.10:g.94522176G>C , CM000663.1:g.94522176G>C | GRCh37 |
NC_000001.9:g.94294764G>C | NCBI36 |
NG_009073.1:g.69530C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2363C>G MANE Select | ENSP00000359245.3:p.Ala788Gly | |
ENST00000649773.1:c.2161-1305C>G | ENSP00000496882.1:n.2161-1305C>G | |
ENST00000370225.3:c.2363C>G | ENSP00000359245.3:p.Ala788Gly | |
ENST00000536513.5:c.-65+6554C>G | ENSP00000439707.2:n.-65+6554C>G | |
NM_000350.2:c.2363C>G | NP_000341.2:p.Ala788Gly | |
NM_000350.3:c.2363C>G MANE Select | NP_000341.2:p.Ala788Gly |