Canonical Allele Identifier: CA778454338
Gene:

Linked Data

dbSNP Id: rs1399086788
gnomAD v3: 18-31756946-G-C
gnomAD v4: 18-31756946-G-C
MyVariant Identifiers: chr18:g.29336909G>C (hg19) chr18:g.31756946G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756946G>C , CM000680.2:g.31756946G>C GRCh38
NC_000018.9:g.29336909G>C , CM000680.1:g.29336909G>C GRCh37
NC_000018.8:g.27590907G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935338.1:n.66-5193G>C
Search 100 bp 5'
Search 100 bp 3'