HGVS | Genome Assembly |
---|---|
NC_000011.10:g.61392396A>G , CM000673.2:g.61392396A>G | GRCh38 |
NC_000011.9:g.61159868A>G , CM000673.1:g.61159868A>G | GRCh37 |
NC_000011.8:g.60916444A>G | NCBI36 |
NG_032976.1:g.5037A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000334888.9:c.-236A>G | ENSP00000334844.5:n.-236A>G | |
ENST00000398979.7:c.-433A>G | ENSP00000381950.3:n.-433A>G | |
ENST00000515837.6:c.-236A>G | ENSP00000440638.1:n.-236A>G | |
NM_001173990.2:c.-236A>G | NP_001167461.1:n.-236A>G | |
NM_001173991.2:c.-236A>G | NP_001167462.1:n.-236A>G | |
NM_016499.5:c.-433A>G | NP_057583.2:n.-433A>G | |
XM_005274039.3:c.-567A>G | XP_005274096.1:n.-567A>G | |
NM_001330285.1:c.-433A>G | NP_001317214.1:n.-433A>G | |
XM_005274039.4:c.-567A>G | XP_005274096.1:n.-567A>G |