HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149981832G= , CM000667.2:g.149981832G= | GRCh38 |
NC_000005.9:g.149361395G= , CM000667.1:g.149361395G= | GRCh37 |
NC_000005.8:g.149341588G= | NCBI36 |
NG_007147.2:g.22950G= , LRG_684:g.22950G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286298.5:c.*19G= MANE Select | ENSP00000286298.4:n.*19G= | |
ENST00000286298.4:c.*19G= | ENSP00000286298.4:n.*19G= | |
ENST00000503336.1:c.372+3481G= | ENSP00000426053.1:n.372+3481G= | |
NM_000112.3:c.*19G= , LRG_684t1:c.*19G= | NP_000103.2:n.*19G= | |
XM_017009191.2:c.*12+7G= | XP_016864680.1:n.*12+7G= | |
NM_000112.4:c.*19G= MANE Select | NP_000103.2:n.*19G= |