HGVS | Genome Assembly |
---|---|
NC_000008.11:g.30786213A>C , CM000670.2:g.30786213A>C | GRCh38 |
NC_000008.10:g.30643729A>C , CM000670.1:g.30643729A>C | GRCh37 |
NC_000008.9:g.30763271A>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000221138.9:c.*22T>G MANE Select | ENSP00000221138.4:n.*22T>G | |
ENST00000221138.8:c.*22T>G | ENSP00000221138.4:n.*22T>G | |
ENST00000518532.1:n.462T>G | ||
ENST00000518564.1:c.142-224T>G | ENSP00000428142.1:n.142-224T>G | |
ENST00000522113.1:n.152T>G | ||
ENST00000523023.1:c.179T>G | ||
NM_001009552.1:c.*22T>G | NP_001009552.1:n.*22T>G | |
NM_001009552.2:c.*22T>G MANE Select | NP_001009552.1:n.*22T>G |