HGVS | Genome Assembly |
---|---|
NC_000001.11:g.45500308G= , CM000663.2:g.45500308G= | GRCh38 |
NC_000001.10:g.45965980G= , CM000663.1:g.45965980G= | GRCh37 |
NC_000001.9:g.45738567G= | NCBI36 |
NG_013378.1:g.5125G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000401061.9:c.-25G= MANE Select | ENSP00000383840.4:n.-25G= | |
ENST00000401061.8:c.-25G= | ENSP00000383840.4:n.-25G= | |
NM_015506.2:c.-25G= | NP_056321.2:n.-25G= | |
NM_001330540.1:c.-247G= | NP_001317469.1:n.-247G= | |
XM_005270724.5:c.-25G= | XP_005270781.1:n.-25G= | |
NM_015506.3:c.-25G= MANE Select | NP_056321.2:n.-25G= | |
NM_001330540.2:c.-247G= | NP_001317469.1:n.-247G= |