HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978337G>T , CM000667.2:g.149978337G>T | GRCh38 |
NC_000005.9:g.149357900G>T , CM000667.1:g.149357900G>T | GRCh37 |
NC_000005.8:g.149338093G>T | NCBI36 |
NG_007147.2:g.19455G>T , LRG_684:g.19455G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000690410.1:n.917G>T | ||
ENST00000286298.5:c.685G>T MANE Select | ENSP00000286298.4:p.Ala229Ser | |
ENST00000286298.4:c.685G>T | ENSP00000286298.4:p.Ala229Ser | |
ENST00000503336.1:c.358G>T | ENSP00000426053.1:p.Ala120Ser | |
NM_000112.3:c.685G>T , LRG_684t1:c.685G>T | NP_000103.2:p.Ala229Ser | |
XM_017009191.2:c.685G>T | XP_016864680.1:p.Ala229Ser | |
NM_000112.4:c.685G>T MANE Select | NP_000103.2:p.Ala229Ser |