HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713499C= , CM000681.2:g.6713499C= | GRCh38 |
NC_000019.9:g.6713510C= , CM000681.1:g.6713510C= | GRCh37 |
NC_000019.8:g.6664510C= | NCBI36 |
NG_009557.1:g.12153G= , LRG_27:g.12153G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.661G= | ENSP00000512083.1:p.Gly221= | |
ENST00000695692.1:n.108G= | ||
ENST00000245907.11:c.784G= MANE Select | ENSP00000245907.4:p.Gly262= | |
ENST00000245907.10:c.784G= | ENSP00000245907.4:p.Gly262= | |
ENST00000595577.1:n.288G= | ||
ENST00000597442.5:n.34G= | ||
NM_000064.3:c.784G= | NP_000055.2:p.Gly262= | |
NM_000064.4:c.784G= MANE Select | NP_000055.2:p.Gly262= |