HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43838956T>G , CM000664.2:g.43838956T>G | GRCh38 |
NC_000002.11:g.44066095T>G , CM000664.1:g.44066095T>G | GRCh37 |
NC_000002.10:g.43919599T>G | NCBI36 |
NG_008883.1:g.4864A>C | |
NG_008884.1:g.4993T>G | |
NG_008884.2:g.12015T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000643284.1:n.521-5551T>G | ||
ENST00000644611.1:c.76-5551T>G | ENSP00000495423.1:n.76-5551T>G | |
XM_011533029.1:c.76-5551T>G | XP_011531331.1:n.76-5551T>G | |
XM_011533030.1:c.76-5551T>G | XP_011531332.1:n.76-5551T>G | |
XM_011533031.1:c.-153-5551T>G | XP_011531333.1:n.-153-5551T>G | |
XR_939707.1:n.566-5551T>G | ||
XM_011533029.2:c.76-5551T>G | XP_011531331.1:n.76-5551T>G | |
XM_011533030.2:c.76-5551T>G | XP_011531332.1:n.76-5551T>G | |
XR_001738891.1:n.580-5551T>G | ||
XR_939707.2:n.580-5551T>G |