HGVS | Genome Assembly |
---|---|
NC_000011.10:g.61392381G>A , CM000673.2:g.61392381G>A | GRCh38 |
NC_000011.9:g.61159853G>A , CM000673.1:g.61159853G>A | GRCh37 |
NC_000011.8:g.60916429G>A | NCBI36 |
NG_032976.1:g.5022G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000334888.9:c.-251G>A | ENSP00000334844.5:n.-251G>A | |
ENST00000515837.6:c.-251G>A | ENSP00000440638.1:n.-251G>A | |
NM_001173990.2:c.-251G>A | NP_001167461.1:n.-251G>A | |
NM_001173991.2:c.-251G>A | NP_001167462.1:n.-251G>A | |
XM_005274039.3:c.-582G>A | XP_005274096.1:n.-582G>A | |
NM_001330285.1:c.-448G>A | NP_001317214.1:n.-448G>A | |
XM_005274039.4:c.-582G>A | XP_005274096.1:n.-582G>A |