Canonical Allele Identifier: CA1649498121
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014520_98014521delinsTG , CM000668.2:g.98014520_98014521delinsTG GRCh38
NC_000006.11:g.98462396_98462397delinsTG , CM000668.1:g.98462396_98462397delinsTG GRCh37
NC_000006.10:g.98569117_98569118delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45054_371+45055delinsTG
XR_942809.1:n.371+45054_371+45055delinsTG