Canonical Allele Identifier: CA1096780351
Gene:

Linked Data

dbSNP Id: rs1780707850

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765645_163765646insGG , CM000668.2:g.163765645_163765646insGG GRCh38
NC_000006.11:g.164186677_164186678insGG , CM000668.1:g.164186677_164186678insGG GRCh37
NC_000006.10:g.164106667_164106668insGG NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001744452.1:n.410+6216_410+6217insGG
XR_001744454.1:n.369+6257_369+6258insGG
XR_001744455.1:n.346+6280_346+6281insGG