HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6709562T>C , CM000681.2:g.6709562T>C | GRCh38 |
NC_000019.9:g.6709573T>C , CM000681.1:g.6709573T>C | GRCh37 |
NC_000019.8:g.6660573T>C | NCBI36 |
NG_009557.1:g.16090A>G , LRG_27:g.16090A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.1722+122A>G | ENSP00000512083.1:n.1722+122A>G | |
ENST00000695654.1:c.969+122A>G | ENSP00000512085.1:n.969+122A>G | |
ENST00000695655.1:c.786+122A>G | ENSP00000512086.1:n.786+122A>G | |
ENST00000695692.1:n.1209+122A>G | ||
ENST00000245907.11:c.1845+122A>G MANE Select | ENSP00000245907.4:n.1845+122A>G | |
ENST00000245907.10:c.1845+122A>G | ENSP00000245907.4:n.1845+122A>G | |
NM_000064.3:c.1845+122A>G | NP_000055.2:n.1845+122A>G | |
NM_000064.4:c.1845+122A>G MANE Select | NP_000055.2:n.1845+122A>G |