Linked Data
dbSNP Id:
rs1469599003
gnomAD v2:
12-6443368-T-A
gnomAD v3:
12-6334202-T-A
gnomAD v4:
12-6334202-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6334202T>A , CM000674.2:g.6334202T>A | GRCh38 |
| NC_000012.11:g.6443368T>A , CM000674.1:g.6443368T>A | GRCh37 |
| NC_000012.10:g.6313629T>A | NCBI36 |
| NG_007506.1:g.12894A>T , LRG_193:g.12894A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366159.9:n.116A>T | ||
| ENST00000437813.8:c.82A>T | ENSP00000513672.1:p.Ile28Phe | |
| ENST00000440083.7:c.82A>T | ENSP00000413224.3:p.Ile28Phe | |
| ENST00000535958.2:c.82A>T | ENSP00000513673.1:p.Ile28Phe | |
| ENST00000698339.1:c.82A>T | ENSP00000513670.1:p.Ile28Phe | |
| ENST00000698340.1:c.82A>T | ENSP00000513671.1:p.Ile28Phe | |
| ENST00000162749.7:c.82A>T MANE Select | ENSP00000162749.2:p.Ile28Phe | |
| ENST00000162749.6:c.82A>T | ENSP00000162749.2:p.Ile28Phe | |
| ENST00000366159.8:c.82A>T | ENSP00000380389.3:p.Ile28Phe | |
| ENST00000437813.7:n.43A>T | ||
| ENST00000440083.6:c.82A>T | ENSP00000413224.2:p.Ile28Phe | |
| ENST00000534885.5:c.40-337A>T | ENSP00000441803.1:n.40-337A>T | |
| ENST00000535958.1:n.303A>T | ||
| ENST00000536194.1:c.82A>T | ENSP00000442919.1:p.Ile28Phe | |
| ENST00000538363.1:n.272A>T | ||
| ENST00000539372.5:c.82A>T | ENSP00000442059.1:p.Ile28Phe | |
| ENST00000540022.5:c.82A>T | ENSP00000438343.1:p.Ile28Phe | |
| ENST00000543048.5:c.82A>T | ENSP00000439981.1:p.Ile28Phe | |
| ENST00000543995.5:c.82A>T | ENSP00000442405.1:p.Ile28Phe | |
| NM_001065.3:c.82A>T , LRG_193t1:c.82A>T | NP_001056.1:p.Ile28Phe | |
| NM_001346091.1:c.-131-337A>T | NP_001333020.1:n.-131-337A>T | |
| NM_001346092.1:c.-496A>T | NP_001333021.1:n.-496A>T | |
| NR_144351.1:n.385A>T | ||
| NM_001065.4:c.82A>T MANE Select | NP_001056.1:p.Ile28Phe | |
| NM_001346091.2:c.-131-337A>T | NP_001333020.1:n.-131-337A>T | |
| NM_001346092.2:c.-496A>T | NP_001333021.1:n.-496A>T | |
| NR_144351.2:n.344A>T |