HGVS | Genome Assembly |
---|---|
NC_000015.10:g.45480322C>T , CM000677.2:g.45480322C>T | GRCh38 |
NC_000015.9:g.45772520C>T , CM000677.1:g.45772520C>T | GRCh37 |
NC_000015.8:g.43559812C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261867.5:c.*4841G>A MANE Select | ENSP00000261867.3:n.*4841G>A | |
ENST00000261867.4:c.*4841G>A | ENSP00000261867.3:n.*4841G>A | |
NM_013309.5:c.*4841G>A | NP_037441.2:n.*4841G>A | |
NM_013309.6:c.*4841G>A MANE Select | NP_037441.2:n.*4841G>A |