Linked Data
dbSNP Id:
rs554555831
ExAC:
7:107350585 A / G
gnomAD v2:
7-107350585-A-G
gnomAD v3:
7-107710140-A-G
gnomAD v4:
7-107710140-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107710140A>G , CM000669.2:g.107710140A>G | GRCh38 |
| NC_000007.13:g.107350585A>G , CM000669.1:g.107350585A>G | GRCh37 |
| NC_000007.12:g.107137821A>G | NCBI36 |
| NG_008489.1:g.54506A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.2176A>G MANE Select | ENSP00000494017.1:p.Ile726Val | |
| ENST00000644846.1:c.832A>G | ||
| ENST00000265715.7:c.2176A>G | ENSP00000265715.3:p.Ile726Val | |
| ENST00000492030.2:n.377-15A>G | ||
| NM_000441.1:c.2176A>G | NP_000432.1:p.Ile726Val | |
| XM_005250425.1:c.2176A>G | XP_005250482.1:p.Ile726Val | |
| XM_005250425.2:c.2176A>G | XP_005250482.1:p.Ile726Val | |
| XM_017012318.1:c.2098A>G | XP_016867807.1:p.Ile700Val | |
| NM_000441.2:c.2176A>G MANE Select | NP_000432.1:p.Ile726Val |