Canonical Allele Identifier:
CA2388529168
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.37560476T>A , CM000683.2:g.37560476T>A | GRCh38 |
| NC_000021.8:g.38932778T>A , CM000683.1:g.38932778T>A | GRCh37 |
| NC_000021.7:g.37854648T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_017028523.1:c.-2950T>A | XP_016884012.1:n.-2950T>A | |
| XR_937706.2:n.458T>A | ||
| XR_005647073.1:n.458T>A |