HGVS | Genome Assembly |
---|---|
NC_000012.12:g.121627264A>G , CM000674.2:g.121627264A>G | GRCh38 |
NC_000012.11:g.122065170A>G , CM000674.1:g.122065170A>G | GRCh37 |
NC_000012.10:g.120549553A>G | NCBI36 |
NG_007500.1:g.5690A>G , LRG_93:g.5690A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698901.1:n.425+331A>G | ||
ENST00000617316.2:c.303+214A>G | ENSP00000482568.2:n.303+214A>G | |
ENST00000646827.1:n.501+214A>G | ||
ENST00000611718.1:c.238+90A>G | ENSP00000477953.1:n.238+90A>G | |
ENST00000616379.1:c.303+214A>G | ENSP00000480616.1:n.303+214A>G | |
ENST00000617316.1:c.114+214A>G | ENSP00000482568.1:n.114+214A>G | |
NM_032790.3:c.303+214A>G , LRG_93t1:c.303+214A>G | NP_116179.2:n.303+214A>G |