HGVS | Genome Assembly |
---|---|
NC_000003.12:g.147413272A>G , CM000665.2:g.147413272A>G | GRCh38 |
NC_000003.11:g.147131059A>G , CM000665.1:g.147131059A>G | GRCh37 |
NC_000003.10:g.148613749A>G | NCBI36 |
NG_015886.1:g.8879A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282928.5:c.1147-82A>G MANE Select | ENSP00000282928.4:n.1147-82A>G | |
ENST00000282928.4:c.1147-82A>G | ENSP00000282928.4:n.1147-82A>G | |
ENST00000472523.1:n.521+19330A>G | ||
ENST00000488404.5:c.213-82A>G | ||
NM_003412.3:c.1147-82A>G | NP_003403.2:n.1147-82A>G | |
NM_003412.4:c.1147-82A>G MANE Select | NP_003403.2:n.1147-82A>G |