HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713576C= , CM000681.2:g.6713576C= | GRCh38 |
NC_000019.9:g.6713587C= , CM000681.1:g.6713587C= | GRCh37 |
NC_000019.8:g.6664587C= | NCBI36 |
NG_009557.1:g.12076G= , LRG_27:g.12076G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.651-67G= | ENSP00000512083.1:n.651-67G= | |
ENST00000695692.1:n.31G= | ||
ENST00000245907.11:c.774-67G= MANE Select | ENSP00000245907.4:n.774-67G= | |
ENST00000245907.10:c.774-67G= | ENSP00000245907.4:n.774-67G= | |
ENST00000595577.1:n.278-67G= | ||
ENST00000597442.5:n.24-67G= | ||
NM_000064.3:c.774-67G= | NP_000055.2:n.774-67G= | |
NM_000064.4:c.774-67G= MANE Select | NP_000055.2:n.774-67G= |