Canonical Allele Identifier:
CA113962996
Gene:
gnomAD v3:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.6879865T>G , CM000667.2:g.6879865T>G | GRCh38 |
| NC_000005.9:g.6879978T>G , CM000667.1:g.6879978T>G | GRCh37 |
| NC_000005.8:g.6932978T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_925741.1:n.117-6561T>G | ||
| XR_001742496.1:n.285-6561T>G | ||
| XR_925741.2:n.151-6561T>G |