HGVS | Genome Assembly |
---|---|
NC_000003.12:g.147413297T= , CM000665.2:g.147413297T= | GRCh38 |
NC_000003.11:g.147131084T= , CM000665.1:g.147131084T= | GRCh37 |
NC_000003.10:g.148613774T= | NCBI36 |
NG_015886.1:g.8904T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282928.5:c.1147-57T= MANE Select | ENSP00000282928.4:n.1147-57T= | |
ENST00000282928.4:c.1147-57T= | ENSP00000282928.4:n.1147-57T= | |
ENST00000472523.1:n.521+19355T= | ||
ENST00000488404.5:c.213-57T= | ||
NM_003412.3:c.1147-57T= | NP_003403.2:n.1147-57T= | |
NM_003412.4:c.1147-57T= MANE Select | NP_003403.2:n.1147-57T= |