HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50911065G>C , CM000685.2:g.50911065G>C | GRCh38 |
NC_000023.10:g.50654065G>C , CM000685.1:g.50654065G>C | GRCh37 |
NC_000023.9:g.50670805G>C | NCBI36 |
NG_012894.1:g.5282G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252677.4:c.282G>C MANE Select | ENSP00000252677.3:p.Met94Ile | |
ENST00000252677.3:c.282G>C | ENSP00000252677.3:p.Met94Ile | |
NM_005448.2:c.282G>C MANE Select | NP_005439.2:p.Met94Ile |