HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013525T>C , CM000685.2:g.25013525T>C | GRCh38 |
NC_000023.10:g.25031642T>C , CM000685.1:g.25031642T>C | GRCh37 |
NC_000023.9:g.24941563T>C | NCBI36 |
NG_008281.1:g.7424A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.470A>G MANE Select | ENSP00000368332.4:p.Asp157Gly | |
ENST00000379044.4:c.470A>G | ENSP00000368332.4:p.Asp157Gly | |
NM_139058.2:c.470A>G | NP_620689.1:p.Asp157Gly | |
NM_139058.3:c.470A>G MANE Select | NP_620689.1:p.Asp157Gly |