HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978079A>G , CM000667.2:g.149978079A>G | GRCh38 |
NC_000005.9:g.149357642A>G , CM000667.1:g.149357642A>G | GRCh37 |
NC_000005.8:g.149337835A>G | NCBI36 |
NG_007147.2:g.19197A>G , LRG_684:g.19197A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.659A>G | ||
ENST00000286298.5:c.427A>G MANE Select | ENSP00000286298.4:p.Thr143Ala | |
ENST00000286298.4:c.427A>G | ENSP00000286298.4:p.Thr143Ala | |
ENST00000503336.1:c.100A>G | ENSP00000426053.1:p.Thr34Ala | |
NM_000112.3:c.427A>G , LRG_684t1:c.427A>G | NP_000103.2:p.Thr143Ala | |
XM_017009191.2:c.427A>G | XP_016864680.1:p.Thr143Ala | |
NM_000112.4:c.427A>G MANE Select | NP_000103.2:p.Thr143Ala |