HGVS | Genome Assembly |
---|---|
NC_000009.12:g.127853890A>G , CM000671.2:g.127853890A>G | GRCh38 |
NC_000009.11:g.130616169A>G , CM000671.1:g.130616169A>G | GRCh37 |
NC_000009.10:g.129655990A>G | NCBI36 |
NG_009551.1:g.5879T>C , LRG_589:g.5879T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373203.9:c.67+399T>C MANE Select | ENSP00000362299.4:n.67+399T>C | |
ENST00000344849.4:c.67+399T>C | ENSP00000341917.3:n.67+399T>C | |
ENST00000373203.8:c.67+399T>C | ENSP00000362299.4:n.67+399T>C | |
NM_000118.3:c.67+399T>C , LRG_589t1:c.67+399T>C | NP_000109.1:n.67+399T>C | |
NM_001114753.2:c.67+399T>C , LRG_589t2:c.67+399T>C | NP_001108225.1:n.67+399T>C | |
NM_001114753.3:c.67+399T>C MANE Select | NP_001108225.1:n.67+399T>C |