Canonical Allele Identifier:
CA327945235
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38140399A>T , CM000685.2:g.38140399A>T | GRCh38 |
| NC_000023.10:g.37999652A>T , CM000685.1:g.37999652A>T | GRCh37 |
| NC_000023.9:g.37884596A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465127.1:c.172-525722A>T | ENSP00000417050.1:n.172-525722A>T |