Canonical Allele Identifier:
CA2685463867
Gene:
Linked Data
gnomAD v4:
7-148807250-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.148807250T>G , CM000669.2:g.148807250T>G | GRCh38 |
| NC_000007.13:g.148504342T>G , CM000669.1:g.148504342T>G | GRCh37 |
| NC_000007.12:g.148135275T>G | NCBI36 |
| NG_032043.1:g.82100A>C , LRG_531:g.82100A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928101.1:n.515+2165T>G | ||
| XR_928102.1:n.722+2165T>G |