Canonical Allele Identifier:
CA440618880
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.103422055C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102500898C>G , CM000666.2:g.102500898C>G | GRCh38 |
| NC_000004.11:g.103422055C>G , CM000666.1:g.103422055C>G | GRCh37 |
| NC_000004.10:g.103641087C>G | NCBI36 |
| NG_050628.1:g.4570C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+351G>C | XP_011530769.1:n.643+351G>C | |
| NR_136202.1:n.48+1541G>C |