Canonical Allele Identifier:
CA671766181
Gene:
Linked Data
dbSNP Id:
rs1291647967
gnomAD v3:
11-112164704-A-AG
gnomAD v4:
11-112164704-A-AG
MyVariant Identifiers:
chr11:g.112035427_112035428insG (hg19)
chr11:g.112164704_112164705insG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112164705dup , CM000673.2:g.112164705dup | GRCh38 |
| NC_000011.9:g.112035428dup , CM000673.1:g.112035428dup | GRCh37 |
| NC_000011.8:g.111540638dup | NCBI36 |
| NG_028143.1:g.4413dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000525987.5:n.320-5714dup | ||
| ENST00000531744.5:c.315-5714dup | ENSP00000456957.1:n.315-5714dup | |
| ENST00000532699.1:c.315-5714dup | ENSP00000456434.1:n.315-5714dup |