HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35805966T>C , CM000668.2:g.35805966T>C | GRCh38 |
NC_000006.11:g.35773743T>C , CM000668.1:g.35773743T>C | GRCh37 |
NC_000006.10:g.35881721T>C | NCBI36 |
NG_012184.1:g.5673T>C | |
NG_012184.2:g.5673T>C | |
NG_012184.3:g.13761T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360215.3:c.296T>C MANE Select | ENSP00000353346.1:p.Phe99Ser | |
ENST00000651132.1:c.296T>C | ENSP00000498322.1:p.Phe99Ser | |
ENST00000651676.1:c.296T>C | ENSP00000498699.1:p.Phe99Ser | |
ENST00000651994.1:c.296T>C | ENSP00000498310.1:p.Phe99Ser | |
ENST00000652718.1:c.128T>C | ENSP00000498866.1:p.Phe43Ser | |
ENST00000360215.2:c.296T>C | ENSP00000353346.1:p.Phe99Ser | |
NM_182548.3:c.296T>C | NP_872354.1:p.Phe99Ser | |
XM_011514403.1:c.296T>C | XP_011512705.1:p.Phe99Ser | |
NM_182548.4:c.296T>C MANE Select | NP_872354.1:p.Phe99Ser |