Canonical Allele Identifier: CA2607210313
Gene:

Linked Data

dbSNP Id: rs2105755317

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033287_200033288insA , CM000664.2:g.200033287_200033288insA GRCh38
NC_000002.11:g.200898010_200898011insA , CM000664.1:g.200898010_200898011insA GRCh37
NC_000002.10:g.200606255_200606256insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22392_178-22391insT