HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107710183G= , CM000669.2:g.107710183G= | GRCh38 |
NC_000007.13:g.107350628G= , CM000669.1:g.107350628G= | GRCh37 |
NC_000007.12:g.107137864G= | NCBI36 |
NG_008489.1:g.54549G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644269.2:c.2219G= MANE Select | ENSP00000494017.1:p.Gly740= | |
ENST00000644846.1:c.875G= | ||
ENST00000265715.7:c.2219G= | ENSP00000265715.3:p.Gly740= | |
ENST00000492030.2:n.405G= | ||
NM_000441.1:c.2219G= | NP_000432.1:p.Gly740= | |
XM_005250425.1:c.2219G= | XP_005250482.1:p.Gly740= | |
XM_005250425.2:c.2219G= | XP_005250482.1:p.Gly740= | |
XM_017012318.1:c.2141G= | XP_016867807.1:p.Gly714= | |
NM_000441.2:c.2219G= MANE Select | NP_000432.1:p.Gly740= |