Canonical Allele Identifier: CA2697393157
Gene:

Linked Data

dbSNP Id: rs2101874812

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649403_168649404insAGTA , CM000663.2:g.168649403_168649404insAGTA GRCh38
NC_000001.10:g.168618641_168618642insAGTA , CM000663.1:g.168618641_168618642insAGTA GRCh37
NC_000001.9:g.166885265_166885266insAGTA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8129_201-8128insTACT
XR_922259.2:n.332-8129_332-8128insTACT