Canonical Allele Identifier: CA1205765971
Gene:

Linked Data

dbSNP Id: rs1648343628

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649321_168649322insT , CM000663.2:g.168649321_168649322insT GRCh38
NC_000001.10:g.168618559_168618560insT , CM000663.1:g.168618559_168618560insT GRCh37
NC_000001.9:g.166885183_166885184insT NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922259.1:n.201-8047_201-8046insA
XR_922259.2:n.332-8047_332-8046insA