HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35805776T>G , CM000668.2:g.35805776T>G | GRCh38 |
NC_000006.11:g.35773553T>G , CM000668.1:g.35773553T>G | GRCh37 |
NC_000006.10:g.35881531T>G | NCBI36 |
NG_012184.1:g.5483T>G | |
NG_012184.2:g.5483T>G | |
NG_012184.3:g.13571T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360215.3:c.106T>G MANE Select | ENSP00000353346.1:p.Phe36Val | |
ENST00000651132.1:c.106T>G | ENSP00000498322.1:p.Phe36Val | |
ENST00000651676.1:c.106T>G | ENSP00000498699.1:p.Phe36Val | |
ENST00000651994.1:c.106T>G | ENSP00000498310.1:p.Phe36Val | |
ENST00000360215.2:c.106T>G | ENSP00000353346.1:p.Phe36Val | |
NM_182548.3:c.106T>G | NP_872354.1:p.Phe36Val | |
XM_011514403.1:c.106T>G | XP_011512705.1:p.Phe36Val | |
NM_182548.4:c.106T>G MANE Select | NP_872354.1:p.Phe36Val |