Linked Data
dbSNP Id:
rs35467185
MyVariant Identifiers:
chr10:g.135340487_135340488insT (hg19)
chr10:g.133526983_133526984insT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.133526985dup , CM000672.2:g.133526985dup | GRCh38 |
| NC_000010.10:g.135340489dup , CM000672.1:g.135340489dup | GRCh37 |
| NC_000010.9:g.135190479dup | NCBI36 |
| NG_008383.1:g.4623dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000463117.6:c.-40+112dup | ENSP00000440689.1:n.-40+112dup | |
| ENST00000541261.1:c.-40+112dup | ENSP00000437799.1:n.-40+112dup |