HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978051T= , CM000667.2:g.149978051T= | GRCh38 |
NC_000005.9:g.149357614T= , CM000667.1:g.149357614T= | GRCh37 |
NC_000005.8:g.149337807T= | NCBI36 |
NG_007147.2:g.19169T= , LRG_684:g.19169T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.631T= | ||
ENST00000286298.5:c.399T= MANE Select | ENSP00000286298.4:p.Ala133= | |
ENST00000286298.4:c.399T= | ENSP00000286298.4:p.Ala133= | |
ENST00000503336.1:c.72T= | ENSP00000426053.1:p.Ala24= | |
NM_000112.3:c.399T= , LRG_684t1:c.399T= | NP_000103.2:p.Ala133= | |
XM_017009191.2:c.399T= | XP_016864680.1:p.Ala133= | |
NM_000112.4:c.399T= MANE Select | NP_000103.2:p.Ala133= |