HGVS | Genome Assembly |
---|---|
NC_000015.10:g.40932053G>T , CM000677.2:g.40932053G>T | GRCh38 |
NC_000015.9:g.41224251G>T , CM000677.1:g.41224251G>T | GRCh37 |
NC_000015.8:g.39011543G>T | NCBI36 |
NG_046974.1:g.7721G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000249749.7:c.659-118G>T MANE Select | ENSP00000249749.5:n.659-118G>T | |
ENST00000249749.6:c.659-118G>T | ENSP00000249749.5:n.659-118G>T | |
ENST00000559440.1:n.888-118G>T | ||
NM_019074.3:c.659-118G>T | NP_061947.1:n.659-118G>T | |
NM_019074.4:c.659-118G>T MANE Select | NP_061947.1:n.659-118G>T |