HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35805967C>A , CM000668.2:g.35805967C>A | GRCh38 |
NC_000006.11:g.35773744C>A , CM000668.1:g.35773744C>A | GRCh37 |
NC_000006.10:g.35881722C>A | NCBI36 |
NG_012184.1:g.5674C>A | |
NG_012184.2:g.5674C>A | |
NG_012184.3:g.13762C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360215.3:c.297C>A MANE Select | ENSP00000353346.1:p.Phe99Leu | |
ENST00000651132.1:c.297C>A | ENSP00000498322.1:p.Phe99Leu | |
ENST00000651676.1:c.297C>A | ENSP00000498699.1:p.Phe99Leu | |
ENST00000651994.1:c.297C>A | ENSP00000498310.1:p.Phe99Leu | |
ENST00000652718.1:c.129C>A | ENSP00000498866.1:p.Phe43Leu | |
ENST00000360215.2:c.297C>A | ENSP00000353346.1:p.Phe99Leu | |
NM_182548.3:c.297C>A | NP_872354.1:p.Phe99Leu | |
XM_011514403.1:c.297C>A | XP_011512705.1:p.Phe99Leu | |
NM_182548.4:c.297C>A MANE Select | NP_872354.1:p.Phe99Leu |