HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013163C>G , CM000685.2:g.25013163C>G | GRCh38 |
NC_000023.10:g.25031280C>G , CM000685.1:g.25031280C>G | GRCh37 |
NC_000023.9:g.24941201C>G | NCBI36 |
NG_008281.1:g.7786G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.832G>C MANE Select | ENSP00000368332.4:p.Ala278Pro | |
ENST00000379044.4:c.832G>C | ENSP00000368332.4:p.Ala278Pro | |
NM_139058.2:c.832G>C | NP_620689.1:p.Ala278Pro | |
NM_139058.3:c.832G>C MANE Select | NP_620689.1:p.Ala278Pro |