HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25004878G>C , CM000685.2:g.25004878G>C | GRCh38 |
NC_000023.10:g.25022995G>C , CM000685.1:g.25022995G>C | GRCh37 |
NC_000023.9:g.24932916G>C | NCBI36 |
NG_008281.1:g.16071C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.1481C>G MANE Select | ENSP00000368332.4:p.Ala494Gly | |
ENST00000636885.1:n.69C>G | ||
ENST00000379044.4:c.1481C>G | ENSP00000368332.4:p.Ala494Gly | |
NM_139058.2:c.1481C>G | NP_620689.1:p.Ala494Gly | |
NM_139058.3:c.1481C>G MANE Select | NP_620689.1:p.Ala494Gly |