Canonical Allele Identifier: CA14496105
Gene:

Linked Data

dbSNP Id: rs146956228
gnomAD v2: 17-8040647-G-A
gnomAD v3: 17-8137329-G-A
gnomAD v4: 17-8137329-G-A
MyVariant Identifiers: chr17:g.8040647G>A (hg19) chr17:g.8137329G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137329G>A , CM000679.2:g.8137329G>A GRCh38
NC_000017.10:g.8040647G>A , CM000679.1:g.8040647G>A GRCh37
NC_000017.9:g.7981372G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1520G>A
XR_934203.1:n.70-2148G>A
XR_934202.2:n.414-1520G>A
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