Canonical Allele Identifier: CA1144226437
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491609_220491610delinsTG , CM000663.2:g.220491609_220491610delinsTG GRCh38
NC_000001.10:g.220664951_220664952delinsTG , CM000663.1:g.220664951_220664952delinsTG GRCh37
NC_000001.9:g.218731574_218731575delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_922615.1:n.256-625_256-624delinsTG
XR_001737822.1:n.557-625_557-624delinsTG