Canonical Allele Identifier: CA1804794088
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269551_97269555delinsAACCC , CM000670.2:g.97269551_97269555delinsAACCC GRCh38
NC_000008.10:g.98281779_98281783delinsAACCC , CM000670.1:g.98281779_98281783delinsAACCC GRCh37
NC_000008.9:g.98350955_98350959delinsAACCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149515_471+149519delinsGGGTT