HGVS | Genome Assembly |
---|---|
NC_000013.11:g.109767007C>A , CM000675.2:g.109767007C>A | GRCh38 |
NC_000013.10:g.110419354C>A , CM000675.1:g.110419354C>A | GRCh37 |
NC_000013.9:g.109217355C>A | NCBI36 |
NG_008154.1:g.24561G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375856.5:c.4013-10699G>T MANE Select | ENSP00000365016.3:n.4013-10699G>T | |
ENST00000375856.4:c.4013-10699G>T | ENSP00000365016.3:n.4013-10699G>T | |
NM_003749.2:c.4013-10699G>T | NP_003740.2:n.4013-10699G>T | |
NM_003749.3:c.4013-10699G>T MANE Select | NP_003740.2:n.4013-10699G>T |