HGVS | Genome Assembly |
---|---|
NC_000002.12:g.113060848T>G , CM000664.2:g.113060848T>G | GRCh38 |
NC_000002.11:g.113818425T>G , CM000664.1:g.113818425T>G | GRCh37 |
NC_000002.10:g.113534896T>G | NCBI36 |
NG_031864.1:g.7211T>G , LRG_730:g.7211T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437409.2:c.30-4T>G | ENSP00000409262.2:n.30-4T>G | |
ENST00000393200.7:c.30-4T>G MANE Select | ENSP00000376896.2:n.30-4T>G | |
ENST00000346807.7:c.30-4T>G | ENSP00000259212.3:n.30-4T>G | |
ENST00000393200.6:c.30-4T>G | ENSP00000376896.2:n.30-4T>G | |
ENST00000437409.1:c.30-4T>G | ENSP00000409262.1:n.30-4T>G | |
NM_012275.2:c.30-4T>G , LRG_730t2:c.30-4T>G | NP_036407.1:n.30-4T>G | |
NM_173170.1:c.30-4T>G , LRG_730t1:c.30-4T>G | NP_775262.1:n.30-4T>G | |
NM_012275.3:c.30-4T>G MANE Select | NP_036407.1:n.30-4T>G |