HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17023004C>A , CM000663.2:g.17023004C>A | GRCh38 |
NC_000001.10:g.17349499C>A , CM000663.1:g.17349499C>A | GRCh37 |
NC_000001.9:g.17222086C>A | NCBI36 |
NG_012340.1:g.36167G>T , LRG_316:g.36167G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463045.3:c.472-274G>T | ENSP00000481376.2:n.472-274G>T | |
ENST00000491274.6:c.601-274G>T | ENSP00000480482.2:n.601-274G>T | |
ENST00000375499.8:c.643-274G>T MANE Select | ENSP00000364649.3:n.643-274G>T | |
ENST00000375499.7:c.643-274G>T | ENSP00000364649.3:n.643-274G>T | |
ENST00000475049.5:n.67+90G>T | ||
ENST00000485092.5:n.33G>T | ||
ENST00000485515.5:n.577-274G>T | ||
NM_003000.2:c.643-274G>T , LRG_316t1:c.643-274G>T | NP_002991.2:n.643-274G>T | |
NM_003000.3:c.643-274G>T MANE Select | NP_002991.2:n.643-274G>T |