Canonical Allele Identifier: CA460228743
Gene:

Linked Data

gnomAD v4: 8-31176779-C-G
MyVariant Identifiers: chr8:g.31034295C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176779C>G , CM000670.2:g.31176779C>G GRCh38
NC_000008.10:g.31034295C>G , CM000670.1:g.31034295C>G GRCh37
NC_000008.9:g.31153837C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949642.1:n.308C>G
XR_949647.1:n.613G>C
XR_949648.1:n.515G>C
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