Canonical Allele Identifier: CA847111444
Gene:

Linked Data

dbSNP Id: rs1284447463
gnomAD v3: 8-126999209-C-CTAA
gnomAD v4: 8-126999209-C-CTAA
MyVariant Identifiers: chr8:g.128011454_128011455insTAA (hg19) chr8:g.126999209_126999210insTAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999209_126999210insTAA , CM000670.2:g.126999209_126999210insTAA GRCh38
NC_000008.10:g.128011454_128011455insTAA , CM000670.1:g.128011454_128011455insTAA GRCh37
NC_000008.9:g.128080636_128080637insTAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-7346_1301-7345insTAA
Search 100 bp 5'
Search 100 bp 3'