Canonical Allele Identifier: CA287548513
Gene:

Linked Data

dbSNP Id: rs544484189
gnomAD v2: 17-8040750-AGAT-A
gnomAD v3: 17-8137432-AGAT-A
gnomAD v4: 17-8137432-AGAT-A
MyVariant Identifiers: chr17:g.8040751_8040753del (hg19) chr17:g.8137433_8137435del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137436_8137438del , CM000679.2:g.8137436_8137438del GRCh38
NC_000017.10:g.8040754_8040756del , CM000679.1:g.8040754_8040756del GRCh37
NC_000017.9:g.7981479_7981481del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1413_183-1411del
XR_934203.1:n.70-2041_70-2039del
XR_934202.2:n.414-1413_414-1411del
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