HGVS | Genome Assembly |
---|---|
NC_000011.10:g.110460823A>G , CM000673.2:g.110460823A>G | GRCh38 |
NC_000011.9:g.110331547A>G , CM000673.1:g.110331547A>G | GRCh37 |
NC_000011.8:g.109836757A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000260270.3:c.441-1531A>G MANE Select | ENSP00000260270.2:n.441-1531A>G | |
ENST00000260270.2:c.441-1531A>G | ENSP00000260270.2:n.441-1531A>G | |
NM_004109.4:c.441-1531A>G | NP_004100.1:n.441-1531A>G | |
NM_004109.5:c.441-1531A>G MANE Select | NP_004100.1:n.441-1531A>G |