HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94079343T>G , CM000663.2:g.94079343T>G | GRCh38 |
NC_000001.10:g.94544899T>G , CM000663.1:g.94544899T>G | GRCh37 |
NC_000001.9:g.94317487T>G | NCBI36 |
NG_009073.1:g.46807A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.1218A>C MANE Select | ENSP00000359245.3:p.Ala406= | |
ENST00000649773.1:c.1218A>C | ENSP00000496882.1:p.Ala406= | |
ENST00000370225.3:c.1218A>C | ENSP00000359245.3:p.Ala406= | |
NM_000350.2:c.1218A>C | NP_000341.2:p.Ala406= | |
NM_000350.3:c.1218A>C MANE Select | NP_000341.2:p.Ala406= |