HGVS | Genome Assembly |
---|---|
NC_000006.12:g.39216012G>A , CM000668.2:g.39216012G>A | GRCh38 |
NC_000006.11:g.39183788G>A , CM000668.1:g.39183788G>A | GRCh37 |
NC_000006.10:g.39291766G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000359534.4:c.186+12914C>T MANE Select | ENSP00000352527.3:n.186+12914C>T | |
ENST00000359534.3:c.186+12914C>T | ENSP00000352527.3:n.186+12914C>T | |
NM_003740.3:c.186+12914C>T | NP_003731.1:n.186+12914C>T | |
XM_005249456.1:c.186+12914C>T | XP_005249513.1:n.186+12914C>T | |
NM_003740.4:c.186+12914C>T MANE Select | NP_003731.1:n.186+12914C>T |