HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21200790T= , CM000674.2:g.21200790T= | GRCh38 |
NC_000012.11:g.21353724T= , CM000674.1:g.21353724T= | GRCh37 |
NC_000012.10:g.21244991T= | NCBI36 |
NG_011745.1:g.74597T= , LRG_1022:g.74597T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.1135+118T= MANE Select | ENSP00000256958.2:n.1135+118T= | |
ENST00000256958.2:c.1135+118T= | ENSP00000256958.2:n.1135+118T= | |
NM_006446.4:c.1135+118T= , LRG_1022t1:c.1135+118T= | NP_006437.3:n.1135+118T= | |
NM_006446.5:c.1135+118T= MANE Select | NP_006437.3:n.1135+118T= |