HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67585195T>G , CM000673.2:g.67585195T>G | GRCh38 |
NC_000011.9:g.67352666T>G , CM000673.1:g.67352666T>G | GRCh37 |
NC_000011.8:g.67109242T>G | NCBI36 |
NG_012075.1:g.6601T>G , LRG_723:g.6601T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.290T>G | ENSP00000381604.1:p.Val97Gly | |
ENST00000398606.10:c.290T>G MANE Select | ENSP00000381607.3:p.Val97Gly | |
ENST00000646888.1:c.*6T>G | ENSP00000494477.1:n.*6T>G | |
ENST00000398603.5:c.290T>G | ENSP00000381604.1:p.Val97Gly | |
ENST00000398606.7:c.290T>G | ENSP00000381607.3:p.Val97Gly | |
ENST00000467591.1:n.401T>G | ||
ENST00000494593.1:n.1085T>G | ||
ENST00000498765.5:c.353T>G | ||
NM_000852.3:c.290T>G , LRG_723t1:c.290T>G | NP_000843.1:p.Val97Gly | |
NM_000852.4:c.290T>G MANE Select | NP_000843.1:p.Val97Gly |