HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107695968T>A , CM000669.2:g.107695968T>A | GRCh38 |
NC_000007.13:g.107336413T>A , CM000669.1:g.107336413T>A | GRCh37 |
NC_000007.12:g.107123649T>A | NCBI36 |
NG_008489.1:g.40334T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.1473T>A MANE Select | ENSP00000494017.1:p.Ile491= | |
ENST00000644846.1:c.184T>A | ||
ENST00000265715.7:c.1473T>A | ENSP00000265715.3:p.Ile491= | |
ENST00000477350.5:n.320T>A | ||
ENST00000480841.5:n.322T>A | ||
ENST00000497446.5:n.488T>A | ||
NM_000441.1:c.1473T>A | NP_000432.1:p.Ile491= | |
XM_005250425.1:c.1473T>A | XP_005250482.1:p.Ile491= | |
XM_005250425.2:c.1473T>A | XP_005250482.1:p.Ile491= | |
XM_017012318.1:c.1395T>A | XP_016867807.1:p.Ile465= | |
NM_000441.2:c.1473T>A MANE Select | NP_000432.1:p.Ile491= |