HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213763G>T , CM000667.2:g.1213763G>T | GRCh38 |
NC_000005.9:g.1213878G>T , CM000667.1:g.1213878G>T | GRCh37 |
NC_000005.8:g.1266878G>T | NCBI36 |
NG_008282.1:g.17169G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304460.11:c.775-190G>T MANE Select | ENSP00000305302.10:n.775-190G>T | |
ENST00000304460.10:c.775-190G>T | ENSP00000305302.10:n.775-190G>T | |
ENST00000515652.5:c.683-190G>T | ENSP00000425701.1:n.683-190G>T | |
NM_001003841.2:c.775-190G>T | NP_001003841.1:n.775-190G>T | |
NM_001003841.3:c.775-190G>T MANE Select | NP_001003841.1:n.775-190G>T |