HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38381468A>G , CM000685.2:g.38381468A>G | GRCh38 |
NC_000023.10:g.38240721A>G , CM000685.1:g.38240721A>G | GRCh37 |
NC_000023.9:g.38125665A>G | NCBI36 |
NG_008471.1:g.33986A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.386+39A>G MANE Select | ENSP00000039007.4:n.386+39A>G | |
ENST00000643344.1:c.*136+39A>G | ENSP00000496606.1:n.*136+39A>G | |
ENST00000039007.4:c.386+39A>G | ENSP00000039007.4:n.386+39A>G | |
ENST00000465127.1:c.172-284653A>G | ENSP00000417050.1:n.172-284653A>G | |
ENST00000488812.1:n.423+39A>G | ||
NM_000531.5:c.386+39A>G | NP_000522.3:n.386+39A>G | |
XM_017029556.1:c.386+39A>G | XP_016885045.1:n.386+39A>G | |
NM_000531.6:c.386+39A>G MANE Select | NP_000522.3:n.386+39A>G |