Canonical Allele Identifier:
CA1704491107
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.45986582A>T , CM000669.2:g.45986582A>T | GRCh38 |
| NC_000007.13:g.46026181A>T , CM000669.1:g.46026181A>T | GRCh37 |
| NC_000007.12:g.45992706A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927237.1:n.720-3951A>T | ||
| XR_927238.1:n.720-3951A>T | ||
| XR_927239.1:n.720-3951A>T | ||
| XR_927240.1:n.719+6555A>T | ||
| XR_001745202.1:n.725-3951A>T | ||
| XR_001745203.1:n.725-3951A>T |