HGVS | Genome Assembly |
---|---|
NC_000008.11:g.30786196T>C , CM000670.2:g.30786196T>C | GRCh38 |
NC_000008.10:g.30643712T>C , CM000670.1:g.30643712T>C | GRCh37 |
NC_000008.9:g.30763254T>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000221138.9:c.*39A>G MANE Select | ENSP00000221138.4:n.*39A>G | |
ENST00000221138.8:c.*39A>G | ENSP00000221138.4:n.*39A>G | |
ENST00000518532.1:n.479A>G | ||
ENST00000518564.1:c.142-207A>G | ENSP00000428142.1:n.142-207A>G | |
ENST00000522113.1:n.169A>G | ||
ENST00000523023.1:c.181+15A>G | ||
NM_001009552.1:c.*39A>G | NP_001009552.1:n.*39A>G | |
NM_001009552.2:c.*39A>G MANE Select | NP_001009552.1:n.*39A>G |