Canonical Allele Identifier: CA175154019
Gene:

Linked Data

dbSNP Id: rs35639726
MyVariant Identifiers: chr8:g.33665877_33665878insAG (hg19) chr8:g.33808359_33808360insAG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808361_33808362dup , CM000670.2:g.33808361_33808362dup GRCh38
NC_000008.10:g.33665879_33665880dup , CM000670.1:g.33665879_33665880dup GRCh37
NC_000008.9:g.33785421_33785422dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11925_240+11926dup
XR_002956701.1:n.240+11925_240+11926dup
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