HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10897287A>C , CM000668.2:g.10897287A>C | GRCh38 |
NC_000006.11:g.10897520A>C , CM000668.1:g.10897520A>C | GRCh37 |
NC_000006.10:g.11005506A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000283141.11:c.337-724A>C MANE Select | ENSP00000283141.6:n.337-724A>C | |
ENST00000283141.10:c.337-724A>C | ENSP00000283141.6:n.337-724A>C | |
ENST00000341041.8:c.337-724A>C | ENSP00000340320.4:n.337-724A>C | |
ENST00000480294.1:c.*299-724A>C | ENSP00000417929.1:n.*299-724A>C | |
ENST00000543878.5:c.334-724A>C | ENSP00000440676.2:n.334-724A>C | |
NM_001040274.2:c.337-724A>C | NP_001035364.2:n.337-724A>C | |
NM_001040274.3:c.337-724A>C MANE Select | NP_001035364.2:n.337-724A>C |