HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67584730T>G , CM000673.2:g.67584730T>G | GRCh38 |
NC_000011.9:g.67352201T>G , CM000673.1:g.67352201T>G | GRCh37 |
NC_000011.8:g.67108777T>G | NCBI36 |
NG_012075.1:g.6136T>G , LRG_723:g.6136T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.190T>G | ENSP00000381604.1:p.Tyr64Asp | |
ENST00000398606.10:c.190T>G MANE Select | ENSP00000381607.3:p.Tyr64Asp | |
ENST00000646888.1:c.83T>G | ENSP00000494477.1:p.Val28Gly | |
ENST00000398603.5:c.190T>G | ENSP00000381604.1:p.Tyr64Asp | |
ENST00000398606.7:c.190T>G | ENSP00000381607.3:p.Tyr64Asp | |
ENST00000489040.1:n.189T>G | ||
ENST00000494593.1:n.620T>G | ||
ENST00000498765.5:c.153T>G | ||
NM_000852.3:c.190T>G , LRG_723t1:c.190T>G | NP_000843.1:p.Tyr64Asp | |
NM_000852.4:c.190T>G MANE Select | NP_000843.1:p.Tyr64Asp |