HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48381333T>G , CM000675.2:g.48381333T>G | GRCh38 |
NC_000013.10:g.48955469T>G , CM000675.1:g.48955469T>G | GRCh37 |
NC_000013.9:g.47853470T>G | NCBI36 |
NG_009009.1:g.82587T>G , LRG_517:g.82587T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.1585T>G MANE Select | ENSP00000267163.4:p.Tyr529Asp | |
ENST00000643064.1:c.84T>G | ||
ENST00000650461.1:c.1585T>G | ENSP00000497193.1:p.Tyr529Asp | |
ENST00000267163.4:c.1585T>G | ENSP00000267163.4:p.Tyr529Asp | |
NM_000321.2:c.1585T>G , LRG_517t1:c.1585T>G | NP_000312.2:p.Tyr529Asp | |
XM_011535171.1:c.1324T>G | XP_011533473.1:p.Tyr442Asp | |
XM_011535171.2:c.1324T>G | XP_011533473.1:p.Tyr442Asp | |
NM_000321.3:c.1585T>G MANE Select | NP_000312.2:p.Tyr529Asp |