HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6709902T>C , CM000681.2:g.6709902T>C | GRCh38 |
NC_000019.9:g.6709913T>C , CM000681.1:g.6709913T>C | GRCh37 |
NC_000019.8:g.6660913T>C | NCBI36 |
NG_009557.1:g.15750A>G , LRG_27:g.15750A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.1564-60A>G | ENSP00000512083.1:n.1564-60A>G | |
ENST00000695654.1:c.811-60A>G | ENSP00000512085.1:n.811-60A>G | |
ENST00000695655.1:c.592-24A>G | ENSP00000512086.1:n.592-24A>G | |
ENST00000695692.1:n.1051-60A>G | ||
ENST00000245907.11:c.1687-60A>G MANE Select | ENSP00000245907.4:n.1687-60A>G | |
ENST00000245907.10:c.1687-60A>G | ENSP00000245907.4:n.1687-60A>G | |
ENST00000600763.1:n.320-60A>G | ||
NM_000064.3:c.1687-60A>G | NP_000055.2:n.1687-60A>G | |
NM_000064.4:c.1687-60A>G MANE Select | NP_000055.2:n.1687-60A>G |