Canonical Allele Identifier:
CA1702348453
Community Standard Title: NC_000007.14:g.41335525C=
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41335525C= , CM000669.2:g.41335525C= | GRCh38 |
| NC_000007.13:g.41375123C= , CM000669.1:g.41375123C= | GRCh37 |
| NC_000007.12:g.41341648C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_927197.1:n.269+2834C= | |
| XR_927197.2:n.252+2834C= | |
| XR_927198.1:n.269+2834C= | |
| XR_927198.2:n.252+2834C= |