Canonical Allele Identifier: CA775632411
Gene:

Linked Data

dbSNP Id: rs1335233893
gnomAD v3: 17-8137748-TC-T
gnomAD v4: 17-8137748-TC-T
MyVariant Identifiers: chr17:g.8041067del (hg19) chr17:g.8137749del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137749del , CM000679.2:g.8137749del GRCh38
NC_000017.10:g.8041067del , CM000679.1:g.8041067del GRCh37
NC_000017.9:g.7981792del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1100del
XR_934203.1:n.70-1728del
XR_934202.2:n.414-1100del
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