Canonical Allele Identifier:
CA440620298
Gene:
Linked Data
MyVariant Identifiers:
chr4:g.103422356A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102501199A>T , CM000666.2:g.102501199A>T | GRCh38 |
| NC_000004.11:g.103422356A>T , CM000666.1:g.103422356A>T | GRCh37 |
| NC_000004.10:g.103641388A>T | NCBI36 |
| NG_050628.1:g.4871A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+50T>A | XP_011530769.1:n.643+50T>A | |
| NR_136202.1:n.48+1240T>A |