HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149977946G= , CM000667.2:g.149977946G= | GRCh38 |
NC_000005.9:g.149357509G= , CM000667.1:g.149357509G= | GRCh37 |
NC_000005.8:g.149337702G= | NCBI36 |
NG_007147.2:g.19064G= , LRG_684:g.19064G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.526G= | ||
ENST00000286298.5:c.294G= MANE Select | ENSP00000286298.4:p.Trp98= | |
ENST00000286298.4:c.294G= | ENSP00000286298.4:p.Trp98= | |
NM_000112.3:c.294G= , LRG_684t1:c.294G= | NP_000103.2:p.Trp98= | |
XM_017009191.2:c.294G= | XP_016864680.1:p.Trp98= | |
NM_000112.4:c.294G= MANE Select | NP_000103.2:p.Trp98= |