HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149980469T= , CM000667.2:g.149980469T= | GRCh38 |
NC_000005.9:g.149360032T= , CM000667.1:g.149360032T= | GRCh37 |
NC_000005.8:g.149340225T= | NCBI36 |
NG_007147.2:g.21587T= , LRG_684:g.21587T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.876T= MANE Select | ENSP00000286298.4:p.His292= | |
ENST00000286298.4:c.876T= | ENSP00000286298.4:p.His292= | |
ENST00000503336.1:c.372+2118T= | ENSP00000426053.1:n.372+2118T= | |
NM_000112.3:c.876T= , LRG_684t1:c.876T= | NP_000103.2:p.His292= | |
XM_017009191.2:c.876T= | XP_016864680.1:p.His292= | |
NM_000112.4:c.876T= MANE Select | NP_000103.2:p.His292= |