HGVS | Genome Assembly |
---|---|
NC_000003.12:g.8745562A>G , CM000665.2:g.8745562A>G | GRCh38 |
NC_000003.11:g.8787248A>G , CM000665.1:g.8787248A>G | GRCh37 |
NC_000003.10:g.8762248A>G | NCBI36 |
NG_008797.2:g.16753A>G , LRG_329:g.16753A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343849.3:c.151A>G MANE Select | ENSP00000341940.2:p.Thr51Ala | |
ENST00000343849.2:c.151A>G | ENSP00000341940.2:p.Thr51Ala | |
ENST00000397368.2:c.151A>G | ENSP00000380525.2:p.Thr51Ala | |
ENST00000472766.1:n.155+11572A>G | ||
NM_001234.4:c.151A>G | NP_001225.1:p.Thr51Ala | |
NM_033337.2:c.151A>G , LRG_329t1:c.151A>G | NP_203123.1:p.Thr51Ala | |
NM_001234.5:c.151A>G | NP_001225.1:p.Thr51Ala | |
NM_033337.3:c.151A>G MANE Select | NP_203123.1:p.Thr51Ala |