Canonical Allele Identifier: CA1305906772
Gene:
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260511_168260512delinsAT , CM000664.2:g.168260511_168260512delinsAT GRCh38
NC_000002.11:g.169117021_169117022delinsAT , CM000664.1:g.169117021_169117022delinsAT GRCh37
NC_000002.10:g.168825267_168825268delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739763.1:n.912-4585_912-4584delinsAT
XR_001739764.1:n.318-4585_318-4584delinsAT
XR_001739765.1:n.436-4585_436-4584delinsAT
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