Canonical Allele Identifier: CA133346632
Gene:

Linked Data

dbSNP Id: rs116076315
gnomAD v2: 6-465942-C-G
gnomAD v3: 6-465942-C-G
gnomAD v4: 6-465942-C-G
MyVariant Identifiers: chr6:g.465942C>G (hg19) chr6:g.465942C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465942C>G , CM000668.2:g.465942C>G GRCh38
NC_000006.11:g.465942C>G , CM000668.1:g.465942C>G GRCh37
NC_000006.10:g.410942C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12217C>G
XR_926365.1:n.2548+12217C>G
XR_001743914.1:n.482-9266C>G
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