HGVS | Genome Assembly |
---|---|
NC_000003.12:g.38464438A= , CM000665.2:g.38464438A= | GRCh38 |
NC_000003.11:g.38505929A= , CM000665.1:g.38505929A= | GRCh37 |
NC_000003.10:g.38480933A= | NCBI36 |
NG_011791.1:g.15140A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000352511.5:c.52+10064A= MANE Select | ENSP00000340361.3:n.52+10064A= | |
ENST00000352511.4:c.52+10064A= | ENSP00000340361.3:n.52+10064A= | |
ENST00000465020.5:n.56+10064A= | ||
NM_001106.3:c.52+10064A= | NP_001097.2:n.52+10064A= | |
XM_005265583.2:c.115+4749A= | XP_005265640.1:n.115+4749A= | |
XM_005265583.3:c.115+4749A= | XP_005265640.1:n.115+4749A= | |
XM_017007514.1:c.94+4770A= | XP_016863003.1:n.94+4770A= | |
XM_017007515.2:c.70+9754A= | XP_016863004.1:n.70+9754A= | |
NM_001106.4:c.52+10064A= MANE Select | NP_001097.2:n.52+10064A= |