HGVS | Genome Assembly |
---|---|
NC_000003.12:g.186853770A>G , CM000665.2:g.186853770A>G | GRCh38 |
NC_000003.11:g.186571559A>G , CM000665.1:g.186571559A>G | GRCh37 |
NC_000003.10:g.188054253A>G | NCBI36 |
NG_021140.1:g.16097A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320741.7:c.215-414A>G (ADIPOQ) MANE Select | ENSP00000320709.2:n.215-414A>G | |
ENST00000320741.6:c.215-414A>G (ADIPOQ) | ENSP00000320709.2:n.215-414A>G | |
ENST00000444204.2:c.215-414A>G (ADIPOQ) | ENSP00000389814.2:n.215-414A>G | |
NM_001177800.1:c.215-414A>G (ADIPOQ) | NP_001171271.1:n.215-414A>G | |
NM_004797.3:c.215-414A>G (ADIPOQ) | NP_004788.1:n.215-414A>G | |
NR_046662.1:n.2086+8T>C (ADIPOQ-AS1) | ||
XM_011513324.1:c.215-414A>G (ADIPOQ) | XP_011511626.1:n.215-414A>G | |
NR_046662.2:n.2215+8T>C (ADIPOQ-AS1) | ||
NM_004797.4:c.215-414A>G (ADIPOQ) MANE Select | NP_004788.1:n.215-414A>G | |
NM_001177800.2:c.215-414A>G (ADIPOQ) | NP_001171271.1:n.215-414A>G |