HGVS | Genome Assembly |
---|---|
NC_000003.12:g.186856375T>C , CM000665.2:g.186856375T>C | GRCh38 |
NC_000003.11:g.186574164T>C , CM000665.1:g.186574164T>C | GRCh37 |
NC_000003.10:g.188056858T>C | NCBI36 |
NG_021140.1:g.18702T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320741.7:c.*1671T>C (ADIPOQ) MANE Select | ENSP00000320709.2:n.*1671T>C | |
ENST00000320741.6:c.*1671T>C (ADIPOQ) | ENSP00000320709.2:n.*1671T>C | |
ENST00000444204.2:c.*1671T>C (ADIPOQ) | ENSP00000389814.2:n.*1671T>C | |
NM_001177800.1:c.*1671T>C (ADIPOQ) | NP_001171271.1:n.*1671T>C | |
NM_004797.3:c.*1671T>C (ADIPOQ) | NP_004788.1:n.*1671T>C | |
XM_011513324.1:c.*1671T>C (ADIPOQ) | XP_011511626.1:n.*1671T>C | |
NR_046662.2:n.137-259A>G (ADIPOQ-AS1) | ||
NM_004797.4:c.*1671T>C (ADIPOQ) MANE Select | NP_004788.1:n.*1671T>C | |
NM_001177800.2:c.*1671T>C (ADIPOQ) | NP_001171271.1:n.*1671T>C |