Canonical Allele Identifier:
CA1091577395
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.88403098C>A , CM000668.2:g.88403098C>A | GRCh38 |
| NC_000006.11:g.89112817C>A , CM000668.1:g.89112817C>A | GRCh37 |
| NC_000006.10:g.89169536C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_942759.1:n.315+38986G>T | ||
| XR_942760.1:n.315+38986G>T | ||
| XR_942761.1:n.315+38986G>T | ||
| XR_942762.1:n.176+38986G>T | ||
| XR_001744248.2:n.330+38986G>T | ||
| XR_001744250.1:n.321+38986G>T | ||
| XR_001744251.1:n.321+38986G>T | ||
| XR_001744252.2:n.321+38986G>T | ||
| XR_001744253.1:n.394+38986G>T | ||
| XR_942759.2:n.321+38986G>T |