HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48520816A= , CM000677.2:g.48520816A= | GRCh38 |
NC_000015.9:g.48813013A= , CM000677.1:g.48813013A= | GRCh37 |
NC_000015.8:g.46600305A= | NCBI36 |
NG_008805.2:g.129973T= , LRG_778:g.129973T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000559133.6:c.990T= | ENSP00000453958.2:p.Asp330= | |
ENST00000674301.2:c.990T= | ENSP00000501333.2:p.Asp330= | |
ENST00000316623.10:c.990T= MANE Select | ENSP00000325527.5:p.Asp330= | |
ENST00000316623.9:c.990T= | ENSP00000325527.5:p.Asp330= | |
ENST00000537463.6:c.636+16895T= | ENSP00000440294.2:n.636+16895T= | |
NM_000138.4:c.990T= , LRG_778t1:c.990T= | NP_000129.3:p.Asp330= | |
NM_000138.5:c.990T= MANE Select | NP_000129.3:p.Asp330= |