HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713244T>A , CM000681.2:g.6713244T>A | GRCh38 |
NC_000019.9:g.6713255T>A , CM000681.1:g.6713255T>A | GRCh37 |
NC_000019.8:g.6664255T>A | NCBI36 |
NG_009557.1:g.12408A>T , LRG_27:g.12408A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.825A>T | ENSP00000512083.1:p.Ala275= | |
ENST00000695654.1:c.72A>T | ENSP00000512085.1:p.Ala24= | |
ENST00000695692.1:n.272A>T | ||
ENST00000245907.11:c.948A>T MANE Select | ENSP00000245907.4:p.Ala316= | |
ENST00000245907.10:c.948A>T | ENSP00000245907.4:p.Ala316= | |
ENST00000594270.5:n.72A>T | ||
ENST00000595577.1:n.452A>T | ||
ENST00000597442.5:n.198A>T | ||
NM_000064.3:c.948A>T | NP_000055.2:p.Ala316= | |
NM_000064.4:c.948A>T MANE Select | NP_000055.2:p.Ala316= |