HGVS | Genome Assembly |
---|---|
NC_000008.11:g.6877803C>A , CM000670.2:g.6877803C>A | GRCh38 |
NC_000008.10:g.6735325C>A , CM000670.1:g.6735325C>A | GRCh37 |
NC_000008.9:g.6722735C>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297439.4:c.55G>T MANE Select | ENSP00000297439.3:p.Ala19Ser | |
ENST00000297439.3:c.55G>T | ENSP00000297439.3:p.Ala19Ser | |
NM_005218.3:c.55G>T | NP_005209.1:p.Ala19Ser | |
NM_005218.4:c.55G>T MANE Select | NP_005209.1:p.Ala19Ser |