Canonical Allele Identifier: CA624727099
Gene:

Linked Data

dbSNP Id: rs1457330949
gnomAD v2: 17-8041133-A-G
gnomAD v3: 17-8137815-A-G
gnomAD v4: 17-8137815-A-G
MyVariant Identifiers: chr17:g.8041133A>G (hg19) chr17:g.8137815A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137815A>G , CM000679.2:g.8137815A>G GRCh38
NC_000017.10:g.8041133A>G , CM000679.1:g.8041133A>G GRCh37
NC_000017.9:g.7981858A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1034A>G
XR_934203.1:n.70-1662A>G
XR_934202.2:n.414-1034A>G
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