Canonical Allele Identifier: CA778454293
Gene:

Linked Data

dbSNP Id: rs1395225579
gnomAD v3: 18-31756890-G-A
gnomAD v4: 18-31756890-G-A
MyVariant Identifiers: chr18:g.29336853G>A (hg19) chr18:g.31756890G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756890G>A , CM000680.2:g.31756890G>A GRCh38
NC_000018.9:g.29336853G>A , CM000680.1:g.29336853G>A GRCh37
NC_000018.8:g.27590851G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5249G>A
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