HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20242443T>C , CM000684.2:g.20242443T>C | GRCh38 |
NC_000022.10:g.20229966T>C , CM000684.1:g.20229966T>C | GRCh37 |
NC_000022.9:g.18609966T>C | NCBI36 |
NG_012176.1:g.30851A>G | |
NG_012176.2:g.30851A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000043402.8:c.690A>G MANE Select | ENSP00000043402.7:p.Thr230= | |
ENST00000043402.7:c.690A>G | ENSP00000043402.7:p.Thr230= | |
ENST00000416372.5:c.749A>G | ||
ENST00000425986.1:c.947A>G | ||
NM_023004.5:c.690A>G | NP_075380.1:p.Thr230= | |
NM_023004.6:c.690A>G MANE Select | NP_075380.1:p.Thr230= |