Canonical Allele Identifier: CA1674885830
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812590_155812591delinsTG , CM000668.2:g.155812590_155812591delinsTG GRCh38
NC_000006.11:g.156133724_156133725delinsTG , CM000668.1:g.156133724_156133725delinsTG GRCh37
NC_000006.10:g.156175416_156175417delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19171_79+19172delinsTG
XR_943146.1:n.645-552_645-551delinsCA
XR_001744423.1:n.699-552_699-551delinsCA
XR_001744424.1:n.79+19171_79+19172delinsTG