Canonical Allele Identifier: CA1004589651
Gene:

Linked Data

dbSNP Id: rs1652357645

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564031_94564032insA , CM000663.2:g.94564031_94564032insA GRCh38
NC_000001.10:g.95029587_95029588insA , CM000663.1:g.95029587_95029588insA GRCh37
NC_000001.9:g.94802175_94802176insA NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+418_461+419insA