HGVS | Genome Assembly |
---|---|
NC_000020.11:g.32822598A>G , CM000682.2:g.32822598A>G | GRCh38 |
NC_000020.10:g.31410404A>G , CM000682.1:g.31410404A>G | GRCh37 |
NC_000020.9:g.30874065A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375571.6:c.-4+2570A>G MANE Select | ENSP00000364721.5:n.-4+2570A>G | |
ENST00000375571.5:c.-4+2570A>G | ENSP00000364721.5:n.-4+2570A>G | |
NM_012325.2:c.-4+2570A>G | NP_036457.1:n.-4+2570A>G | |
XM_011528696.1:c.-4+2681A>G | XP_011526998.1:n.-4+2681A>G | |
XM_011528696.2:c.-4+2681A>G | XP_011526998.1:n.-4+2681A>G | |
NM_012325.3:c.-4+2570A>G MANE Select | NP_036457.1:n.-4+2570A>G |