HGVS | Genome Assembly |
---|---|
NC_000023.11:g.21845358C>G , CM000685.2:g.21845358C>G | GRCh38 |
NC_000023.10:g.21863476C>G , CM000685.1:g.21863476C>G | GRCh37 |
NC_000023.9:g.21773397C>G | NCBI36 |
NG_012797.1:g.10821C>G | |
NG_012797.2:g.10821C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379484.10:c.412C>G MANE Select | ENSP00000368798.5:p.His138Asp | |
ENST00000365779.2:c.412C>G | ENSP00000368796.1:p.His138Asp | |
ENST00000379484.9:c.412C>G | ENSP00000368798.5:p.His138Asp | |
ENST00000465888.1:n.511C>G | ||
NM_015884.3:c.412C>G | NP_056968.1:p.His138Asp | |
NM_015884.4:c.412C>G MANE Select | NP_056968.1:p.His138Asp |