HGVS | Genome Assembly |
---|---|
NC_000012.12:g.121627175G>T , CM000674.2:g.121627175G>T | GRCh38 |
NC_000012.11:g.122065081G>T , CM000674.1:g.122065081G>T | GRCh37 |
NC_000012.10:g.120549464G>T | NCBI36 |
NG_007500.1:g.5601G>T , LRG_93:g.5601G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698901.1:n.425+242G>T | ||
ENST00000617316.2:c.303+125G>T | ENSP00000482568.2:n.303+125G>T | |
ENST00000646827.1:n.501+125G>T | ||
ENST00000611718.1:c.238+1G>T | ENSP00000477953.1:n.238+1G>T | |
ENST00000616379.1:c.303+125G>T | ENSP00000480616.1:n.303+125G>T | |
ENST00000617316.1:c.114+125G>T | ENSP00000482568.1:n.114+125G>T | |
NM_032790.3:c.303+125G>T , LRG_93t1:c.303+125G>T | NP_116179.2:n.303+125G>T |