Canonical Allele Identifier:
CA2685463868
Gene:
Linked Data
gnomAD v4:
7-148807252-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.148807252C>T , CM000669.2:g.148807252C>T | GRCh38 |
| NC_000007.13:g.148504344C>T , CM000669.1:g.148504344C>T | GRCh37 |
| NC_000007.12:g.148135277C>T | NCBI36 |
| NG_032043.1:g.82098G>A , LRG_531:g.82098G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928101.1:n.515+2167C>T | ||
| XR_928102.1:n.722+2167C>T |