HGVS | Genome Assembly |
---|---|
NC_000015.10:g.48496138T= , CM000677.2:g.48496138T= | GRCh38 |
NC_000015.9:g.48788335T= , CM000677.1:g.48788335T= | GRCh37 |
NC_000015.8:g.46575627T= | NCBI36 |
NG_008805.2:g.154651A= , LRG_778:g.154651A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000559133.6:c.2381A= | ENSP00000453958.2:p.Lys794= | |
ENST00000674301.2:c.2381A= | ENSP00000501333.2:p.Lys794= | |
ENST00000684448.1:n.1055A= | ||
ENST00000316623.10:c.2381A= MANE Select | ENSP00000325527.5:p.Lys794= | |
ENST00000316623.9:c.2381A= | ENSP00000325527.5:p.Lys794= | |
ENST00000537463.6:c.637-21488A= | ENSP00000440294.2:n.637-21488A= | |
NM_000138.4:c.2381A= , LRG_778t1:c.2381A= | NP_000129.3:p.Lys794= | |
NM_000138.5:c.2381A= MANE Select | NP_000129.3:p.Lys794= |