HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6709585G>T , CM000681.2:g.6709585G>T | GRCh38 |
NC_000019.9:g.6709596G>T , CM000681.1:g.6709596G>T | GRCh37 |
NC_000019.8:g.6660596G>T | NCBI36 |
NG_009557.1:g.16067C>A , LRG_27:g.16067C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000695652.1:c.1722+99C>A | ENSP00000512083.1:n.1722+99C>A | |
ENST00000695654.1:c.969+99C>A | ENSP00000512085.1:n.969+99C>A | |
ENST00000695655.1:c.786+99C>A | ENSP00000512086.1:n.786+99C>A | |
ENST00000695692.1:n.1209+99C>A | ||
ENST00000245907.11:c.1845+99C>A MANE Select | ENSP00000245907.4:n.1845+99C>A | |
ENST00000245907.10:c.1845+99C>A | ENSP00000245907.4:n.1845+99C>A | |
NM_000064.3:c.1845+99C>A | NP_000055.2:n.1845+99C>A | |
NM_000064.4:c.1845+99C>A MANE Select | NP_000055.2:n.1845+99C>A |