HGVS | Genome Assembly |
---|---|
NC_000010.11:g.114045231T= , CM000672.2:g.114045231T= | GRCh38 |
NC_000010.10:g.115804990T= , CM000672.1:g.115804990T= | GRCh37 |
NC_000010.9:g.115794980T= | NCBI36 |
NG_012187.1:g.6185T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369295.4:c.1099T= MANE Select | ENSP00000358301.2:p.Tyr367= | |
ENST00000369295.3:c.1099T= | ENSP00000358301.2:p.Tyr367= | |
NM_000684.2:c.1099T= | NP_000675.1:p.Tyr367= | |
NM_000684.3:c.1099T= MANE Select | NP_000675.1:p.Tyr367= |