HGVS | Genome Assembly |
---|---|
NC_000006.12:g.10897345G>A , CM000668.2:g.10897345G>A | GRCh38 |
NC_000006.11:g.10897578G>A , CM000668.1:g.10897578G>A | GRCh37 |
NC_000006.10:g.11005564G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000283141.11:c.337-666G>A MANE Select | ENSP00000283141.6:n.337-666G>A | |
ENST00000283141.10:c.337-666G>A | ENSP00000283141.6:n.337-666G>A | |
ENST00000341041.8:c.337-666G>A | ENSP00000340320.4:n.337-666G>A | |
ENST00000480294.1:c.*299-666G>A | ENSP00000417929.1:n.*299-666G>A | |
ENST00000543878.5:c.334-666G>A | ENSP00000440676.2:n.334-666G>A | |
NM_001040274.2:c.337-666G>A | NP_001035364.2:n.337-666G>A | |
NM_001040274.3:c.337-666G>A MANE Select | NP_001035364.2:n.337-666G>A |