Canonical Allele Identifier:
CA784579002
Gene:
Linked Data
dbSNP Id:
rs1406465305
MyVariant Identifiers:
chr4:g.103420838_103420839insCCTT (hg19)
chr4:g.102499681_102499682insCCTT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499684_102499685insTCCT , CM000666.2:g.102499684_102499685insTCCT | GRCh38 |
| NC_000004.11:g.103420841_103420842insTCCT , CM000666.1:g.103420841_103420842insTCCT | GRCh37 |
| NC_000004.10:g.103639873_103639874insTCCT | NCBI36 |
| NG_050628.1:g.3356_3357insTCCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1567_643+1568insAAGG | XP_011530769.1:n.643+1567_643+1568insAAGG | |
| NR_136202.1:n.48+2757_48+2758insAAGG |