HGVS | Genome Assembly |
---|---|
NC_000008.11:g.100317981A>C , CM000670.2:g.100317981A>C | GRCh38 |
NC_000008.10:g.101330209A>C , CM000670.1:g.101330209A>C | GRCh37 |
NC_000008.9:g.101399385A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000519527.5:c.-242-4609T>G | ENSP00000431077.1:n.-242-4609T>G | |
ENST00000522182.1:n.112-4609T>G | ||
ENST00000522369.5:c.-175-4609T>G | ENSP00000429841.1:n.-175-4609T>G | |
ENST00000616528.1:c.-97-29710T>G | ENSP00000480369.1:n.-97-29710T>G | |
NM_001280539.1:c.-175-4609T>G | NP_001267468.1:n.-175-4609T>G | |
NM_001280539.2:c.-175-4609T>G | NP_001267468.1:n.-175-4609T>G |