HGVS | Genome Assembly |
---|---|
NC_000003.12:g.9890796T>G , CM000665.2:g.9890796T>G | GRCh38 |
NC_000003.11:g.9932480T>G , CM000665.1:g.9932480T>G | GRCh37 |
NC_000003.10:g.9907480T>G | NCBI36 |
NG_041779.1:g.5210T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000489724.2:c.74T>G | ENSP00000497724.1:p.Met25Arg | |
ENST00000647897.1:c.74T>G MANE Select | ENSP00000496942.1:p.Met25Arg | |
ENST00000307768.4:c.74T>G | ENSP00000306106.4:p.Met25Arg | |
ENST00000489724.1:n.164T>G | ||
ENST00000616966.2:c.74T>G | ENSP00000481606.1:p.Met25Arg | |
NM_032492.3:c.74T>G | NP_115881.3:p.Met25Arg | |
NM_001363890.1:c.-195T>G | NP_001350819.1:n.-195T>G | |
NM_032492.4:c.74T>G MANE Select | NP_115881.3:p.Met25Arg |