HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431526A>C , CM000663.2:g.229431526A>C | GRCh38 |
NC_000001.10:g.229567273A>C , CM000663.1:g.229567273A>C | GRCh37 |
NC_000001.9:g.227633896A>C | NCBI36 |
NG_006672.1:g.7571T>G , LRG_429:g.7571T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.1029T>G | ENSP00000355644.4:p.Pro343= | |
ENST00000684723.1:c.972T>G | ENSP00000508084.1:p.Pro324= | |
ENST00000366683.3:c.738T>G | ENSP00000355644.3:p.Pro246= | |
ENST00000366684.7:c.1107T>G MANE Select | ENSP00000355645.3:p.Pro369= | |
NM_001100.3:c.1107T>G , LRG_429t1:c.1107T>G | NP_001091.1:p.Pro369= | |
NM_001100.4:c.1107T>G MANE Select | NP_001091.1:p.Pro369= |