HGVS | Genome Assembly |
---|---|
NC_000003.12:g.73586827T>C , CM000665.2:g.73586827T>C | GRCh38 |
NC_000003.11:g.73635978T>C , CM000665.1:g.73635978T>C | GRCh37 |
NC_000003.10:g.73718668T>C | NCBI36 |
NG_047128.1:g.43095A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263666.9:c.918+15527A>G MANE Select | ENSP00000263666.4:n.918+15527A>G | |
ENST00000263666.8:c.918+15527A>G | ENSP00000263666.4:n.918+15527A>G | |
ENST00000308537.4:c.918+15527A>G | ENSP00000308831.4:n.918+15527A>G | |
NM_015009.2:c.918+15527A>G | NP_055824.1:n.918+15527A>G | |
XM_017005942.2:c.831+15527A>G | XP_016861431.1:n.831+15527A>G | |
NM_015009.3:c.918+15527A>G MANE Select | NP_055824.1:n.918+15527A>G |