HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107696039T= , CM000669.2:g.107696039T= | GRCh38 |
NC_000007.13:g.107336484T= , CM000669.1:g.107336484T= | GRCh37 |
NC_000007.12:g.107123720T= | NCBI36 |
NG_008489.1:g.40405T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.1544T= MANE Select | ENSP00000494017.1:p.Phe515= | |
ENST00000644846.1:c.255T= | ||
ENST00000265715.7:c.1544T= | ENSP00000265715.3:p.Phe515= | |
ENST00000477350.5:n.391T= | ||
ENST00000480841.5:n.393T= | ||
ENST00000497446.5:n.559T= | ||
NM_000441.1:c.1544T= | NP_000432.1:p.Phe515= | |
XM_005250425.1:c.1544T= | XP_005250482.1:p.Phe515= | |
XM_005250425.2:c.1544T= | XP_005250482.1:p.Phe515= | |
XM_017012318.1:c.1466T= | XP_016867807.1:p.Phe489= | |
NM_000441.2:c.1544T= MANE Select | NP_000432.1:p.Phe515= |