HGVS | Genome Assembly |
---|---|
NC_000023.11:g.21845193G>C , CM000685.2:g.21845193G>C | GRCh38 |
NC_000023.10:g.21863311G>C , CM000685.1:g.21863311G>C | GRCh37 |
NC_000023.9:g.21773232G>C | NCBI36 |
NG_012797.1:g.10656G>C | |
NG_012797.2:g.10656G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379484.10:c.247G>C MANE Select | ENSP00000368798.5:p.Gly83Arg | |
ENST00000365779.2:c.247G>C | ENSP00000368796.1:p.Gly83Arg | |
ENST00000379484.9:c.247G>C | ENSP00000368798.5:p.Gly83Arg | |
ENST00000465888.1:n.346G>C | ||
NM_015884.3:c.247G>C | NP_056968.1:p.Gly83Arg | |
NM_015884.4:c.247G>C MANE Select | NP_056968.1:p.Gly83Arg |