Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107701884A>T , CM000669.2:g.107701884A>T | GRCh38 |
| NC_000007.13:g.107342329A>T , CM000669.1:g.107342329A>T | GRCh37 |
| NC_000007.12:g.107129565A>T | NCBI36 |
| NG_008489.1:g.46250A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000644269.2:c.1861A>T MANE Select | ENSP00000494017.1:p.Ile621Phe | |
| ENST00000644846.1:c.572A>T | ||
| ENST00000265715.7:c.1861A>T | ENSP00000265715.3:p.Ile621Phe | |
| ENST00000480841.5:n.710A>T | ||
| ENST00000492030.2:n.148A>T | ||
| NM_000441.1:c.1861A>T | NP_000432.1:p.Ile621Phe | |
| XM_005250425.1:c.1861A>T | XP_005250482.1:p.Ile621Phe | |
| XM_005250425.2:c.1861A>T | XP_005250482.1:p.Ile621Phe | |
| XM_017012318.1:c.1783A>T | XP_016867807.1:p.Ile595Phe | |
| NM_000441.2:c.1861A>T MANE Select | NP_000432.1:p.Ile621Phe |