Canonical Allele Identifier: CA571581106
Gene:

Linked Data

dbSNP Id: rs1175826882
gnomAD v2: 6-156133575-T-TC
gnomAD v3: 6-155812441-T-TC
gnomAD v4: 6-155812441-T-TC
MyVariant Identifiers: chr6:g.156133575_156133576insC (hg19) chr6:g.155812441_155812442insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812446dup , CM000668.2:g.155812446dup GRCh38
NC_000006.11:g.156133580dup , CM000668.1:g.156133580dup GRCh37
NC_000006.10:g.156175272dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19027dup
XR_943146.1:n.645-403dup
XR_001744423.1:n.699-403dup
XR_001744424.1:n.79+19027dup
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