HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38369747del , CM000685.2:g.38369747del | GRCh38 |
NC_000023.10:g.38229000del , CM000685.1:g.38229000del | GRCh37 |
NC_000023.9:g.38113944del | NCBI36 |
NG_008471.1:g.22265del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000039007.5:c.217-49del MANE Select | ENSP00000039007.4:n.217-49del | |
ENST00000643344.1:c.217-49del | ENSP00000496606.1:n.217-49del | |
ENST00000039007.4:c.217-49del | ENSP00000039007.4:n.217-49del | |
ENST00000465127.1:c.172-296374del | ENSP00000417050.1:n.172-296374del | |
ENST00000488812.1:n.309-49del | ||
NM_000531.5:c.217-49del | NP_000522.3:n.217-49del | |
XM_017029556.1:c.217-49del | XP_016885045.1:n.217-49del | |
NM_000531.6:c.217-49del MANE Select | NP_000522.3:n.217-49del |