HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713259C= , CM000681.2:g.6713259C= | GRCh38 |
NC_000019.9:g.6713270C= , CM000681.1:g.6713270C= | GRCh37 |
NC_000019.8:g.6664270C= | NCBI36 |
NG_009557.1:g.12393G= , LRG_27:g.12393G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695652.1:c.810G= | ENSP00000512083.1:p.Val270= | |
ENST00000695654.1:c.57G= | ENSP00000512085.1:p.Val19= | |
ENST00000695692.1:n.257G= | ||
ENST00000245907.11:c.933G= MANE Select | ENSP00000245907.4:p.Val311= | |
ENST00000245907.10:c.933G= | ENSP00000245907.4:p.Val311= | |
ENST00000594270.5:n.57G= | ||
ENST00000595577.1:n.437G= | ||
ENST00000597442.5:n.183G= | ||
NM_000064.3:c.933G= | NP_000055.2:p.Val311= | |
NM_000064.4:c.933G= MANE Select | NP_000055.2:p.Val311= |