Linked Data
dbSNP Id:
rs182455004
ExAC:
11:17574874 T / A
gnomAD v2:
11-17574874-T-A
gnomAD v3:
11-17553327-T-A
gnomAD v4:
11-17553327-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17553327T>A , CM000673.2:g.17553327T>A | GRCh38 |
| NC_000011.9:g.17574874T>A , CM000673.1:g.17574874T>A | GRCh37 |
| NC_000011.8:g.17531450T>A | NCBI36 |
| NG_033191.1:g.10955T>A | |
| NG_033191.2:g.10955T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399391.7:c.422-38T>A | ENSP00000382323.2:n.422-38T>A | |
| ENST00000399397.6:c.386-38T>A MANE Select | ENSP00000382329.2:n.386-38T>A | |
| ENST00000399391.6:c.422-38T>A | ENSP00000382323.2:n.422-38T>A | |
| ENST00000399397.5:c.386-38T>A | ENSP00000382329.2:n.386-38T>A | |
| ENST00000428619.1:c.203-38T>A | ENSP00000399057.2:n.203-38T>A | |
| ENST00000498332.5:n.292-38T>A | ||
| NM_001277269.1:c.422-38T>A | NP_001264198.1:n.422-38T>A | |
| NM_001292063.1:c.386-38T>A | NP_001278992.1:n.386-38T>A | |
| NM_001277269.2:c.422-38T>A | NP_001264198.1:n.422-38T>A | |
| NM_001292063.2:c.386-38T>A MANE Select | NP_001278992.1:n.386-38T>A |