HGVS | Genome Assembly |
---|---|
NC_000023.11:g.50916260G>C , CM000685.2:g.50916260G>C | GRCh38 |
NC_000023.10:g.50659260G>C , CM000685.1:g.50659260G>C | GRCh37 |
NC_000023.9:g.50676000G>C | NCBI36 |
NG_012894.1:g.10477G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252677.4:c.832G>C MANE Select | ENSP00000252677.3:p.Ala278Pro | |
ENST00000252677.3:c.832G>C | ENSP00000252677.3:p.Ala278Pro | |
NM_005448.2:c.832G>C MANE Select | NP_005439.2:p.Ala278Pro |