HGVS | Genome Assembly |
---|---|
NC_000023.11:g.78118321C>T , CM000685.2:g.78118321C>T | GRCh38 |
NC_000023.10:g.77373818C>T , CM000685.1:g.77373818C>T | GRCh37 |
NC_000023.9:g.77260474C>T | NCBI36 |
NG_008862.1:g.19153C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373316.5:c.641+151C>T MANE Select | ENSP00000362413.4:n.641+151C>T | |
ENST00000644362.1:c.557+151C>T | ENSP00000496140.1:n.557+151C>T | |
ENST00000373316.4:c.641+151C>T | ENSP00000362413.4:n.641+151C>T | |
ENST00000491291.1:n.633+151C>T | ||
NM_000291.3:c.641+151C>T | NP_000282.1:n.641+151C>T | |
NM_000291.4:c.641+151C>T MANE Select | NP_000282.1:n.641+151C>T |