Canonical Allele Identifier:
CA553826991
Community Standard Title: NC_000004.12:g.104923116T>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.104923116T>C , CM000666.2:g.104923116T>C | GRCh38 |
| NC_000004.11:g.105844273T>C , CM000666.1:g.105844273T>C | GRCh37 |
| NC_000004.10:g.106063722T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_939034.1:n.79-495T>C | |
| XR_939035.1:n.79-495T>C |