HGVS | Genome Assembly |
---|---|
NC_000013.11:g.109767139G>C , CM000675.2:g.109767139G>C | GRCh38 |
NC_000013.10:g.110419486G>C , CM000675.1:g.110419486G>C | GRCh37 |
NC_000013.9:g.109217487G>C | NCBI36 |
NG_008154.1:g.24429C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375856.5:c.4013-10831C>G MANE Select | ENSP00000365016.3:n.4013-10831C>G | |
ENST00000375856.4:c.4013-10831C>G | ENSP00000365016.3:n.4013-10831C>G | |
NM_003749.2:c.4013-10831C>G | NP_003740.2:n.4013-10831C>G | |
NM_003749.3:c.4013-10831C>G MANE Select | NP_003740.2:n.4013-10831C>G |