Canonical Allele Identifier:
CA11784278
Gene:
Linked Data
dbSNP Id:
rs77169992
gnomAD v2:
4-90577044-C-T
gnomAD v3:
4-89655893-C-T
gnomAD v4:
4-89655893-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.89655893C>T , CM000666.2:g.89655893C>T | GRCh38 |
| NC_000004.11:g.90577044C>T , CM000666.1:g.90577044C>T | GRCh37 |
| NC_000004.10:g.90796067C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938986.1:n.434+27976C>T | ||
| XR_938987.1:n.688+27976C>T | ||
| XR_938988.1:n.554+27976C>T | ||
| XR_938990.1:n.299-35392C>T | ||
| XR_938991.1:n.434+27976C>T | ||
| XR_938994.1:n.779+27976C>T | ||
| XR_938995.1:n.613+27976C>T | ||
| XR_938986.2:n.459+27976C>T | ||
| XR_938987.2:n.748+27976C>T |