HGVS | Genome Assembly |
---|---|
NC_000001.11:g.201915824T>C , CM000663.2:g.201915824T>C | GRCh38 |
NC_000001.10:g.201884952T>C , CM000663.1:g.201884952T>C | GRCh37 |
NC_000001.9:g.200151575T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367288.5:c.262-15073A>G MANE Select | ENSP00000356257.4:n.262-15073A>G | |
ENST00000367288.4:c.262-15073A>G | ENSP00000356257.4:n.262-15073A>G | |
ENST00000616739.1:c.178-15073A>G | ENSP00000480209.1:n.178-15073A>G | |
NM_012134.2:c.262-15073A>G | NP_036266.2:n.262-15073A>G | |
NM_012134.3:c.262-15073A>G MANE Select | NP_036266.2:n.262-15073A>G |