HGVS | Genome Assembly |
---|---|
NC_000017.11:g.39665811T>C , CM000679.2:g.39665811T>C | GRCh38 |
NC_000017.10:g.37822064T>C , CM000679.1:g.37822064T>C | GRCh37 |
NC_000017.9:g.35075590T>C | NCBI36 |
NG_008892.1:g.5466T>C , LRG_210:g.5466T>C | |
NG_042278.1:g.2831T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309889.3:c.206T>C MANE Select | ENSP00000312624.2:p.Met69Thr | |
ENST00000309889.2:c.206T>C | ENSP00000312624.2:p.Met69Thr | |
ENST00000578283.1:c.174+32T>C | ENSP00000462787.1:n.174+32T>C | |
NM_003673.3:c.206T>C , LRG_210t1:c.206T>C | NP_003664.1:p.Met69Thr | |
NM_003673.4:c.206T>C MANE Select | NP_003664.1:p.Met69Thr |