HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169541126A>C , CM000663.2:g.169541126A>C | GRCh38 |
NC_000001.10:g.169510364A>C , CM000663.1:g.169510364A>C | GRCh37 |
NC_000001.9:g.167776988A>C | NCBI36 |
NG_011806.1:g.50406T>G , LRG_553:g.50406T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367797.9:c.3964T>G MANE Select | ENSP00000356771.3:p.Ser1322Ala | |
ENST00000367796.3:c.3979T>G | ENSP00000356770.3:p.Ser1327Ala | |
ENST00000367797.7:c.3964T>G | ENSP00000356771.3:p.Ser1322Ala | |
NM_000130.4:c.3964T>G , LRG_553t1:c.3964T>G | NP_000121.2:p.Ser1322Ala | |
XM_017000660.2:c.3553T>G | XP_016856149.1:p.Ser1185Ala | |
NM_000130.5:c.3964T>G MANE Select | NP_000121.2:p.Ser1322Ala |