HGVS | Genome Assembly |
---|---|
NC_000008.11:g.42838881C= , CM000670.2:g.42838881C= | GRCh38 |
NC_000008.10:g.42694024C= , CM000670.1:g.42694024C= | GRCh37 |
NC_000008.9:g.42813181C= | NCBI36 |
NG_011837.1:g.9451G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000254250.7:c.267+305G= MANE Select | ENSP00000254250.3:n.267+305G= | |
ENST00000345117.2:c.72-545G= | ENSP00000344966.2:n.72-545G= | |
ENST00000529779.1:c.267+305G= | ENSP00000433912.1:n.267+305G= | |
NM_018105.2:c.267+305G= | NP_060575.1:n.267+305G= | |
NM_199003.1:c.72-545G= | NP_945354.1:n.72-545G= | |
NM_018105.3:c.267+305G= MANE Select | NP_060575.1:n.267+305G= | |
NM_199003.2:c.72-545G= | NP_945354.1:n.72-545G= |