gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31271472A>C , CM000668.2:g.31271472A>C | GRCh38 |
| NC_000006.11:g.31239249A>C , CM000668.1:g.31239249A>C | GRCh37 |
| NC_000006.10:g.31347228A>C | NCBI36 |
| NG_029422.2:g.5660T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.344-124T>G MANE Select | ENSP00000365402.5:n.344-124T>G | |
| ENST00000376228.9:c.344-124T>G | ENSP00000365402.5:n.344-124T>G | |
| ENST00000376237.8:c.343+127T>G | ENSP00000365412.4:n.343+127T>G | |
| ENST00000383329.7:c.344-124T>G | ENSP00000372819.3:n.344-124T>G | |
| ENST00000415537.1:c.342-124T>G | ||
| ENST00000484378.1:n.489T>G | ||
| ENST00000487245.5:n.579T>G | ||
| ENST00000495835.1:n.533-124T>G | ||
| NM_002117.5:c.344-124T>G | NP_002108.4:n.344-124T>G | |
| NM_002117.6:c.344-124T>G MANE Select | NP_002108.4:n.344-124T>G |