HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149978271A>T , CM000667.2:g.149978271A>T | GRCh38 |
NC_000005.9:g.149357834A>T , CM000667.1:g.149357834A>T | GRCh37 |
NC_000005.8:g.149338027A>T | NCBI36 |
NG_007147.2:g.19389A>T , LRG_684:g.19389A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000690410.1:n.851A>T | ||
ENST00000286298.5:c.619A>T MANE Select | ENSP00000286298.4:p.Thr207Ser | |
ENST00000286298.4:c.619A>T | ENSP00000286298.4:p.Thr207Ser | |
ENST00000503336.1:c.292A>T | ENSP00000426053.1:p.Thr98Ser | |
NM_000112.3:c.619A>T , LRG_684t1:c.619A>T | NP_000103.2:p.Thr207Ser | |
XM_017009191.2:c.619A>T | XP_016864680.1:p.Thr207Ser | |
NM_000112.4:c.619A>T MANE Select | NP_000103.2:p.Thr207Ser |