Canonical Allele Identifier: CA692802599
Gene:

Linked Data

dbSNP Id: rs1365938886
gnomAD v3: 12-84952071-C-G
gnomAD v4: 12-84952071-C-G
MyVariant Identifiers: chr12:g.85345850C>G (hg19) chr12:g.84952071C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84952071C>G , CM000674.2:g.84952071C>G GRCh38
NC_000012.11:g.85345850C>G , CM000674.1:g.85345850C>G GRCh37
NC_000012.10:g.83869981C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30757C>G
XR_945153.1:n.301+13607C>G
XR_945154.1:n.175-36871C>G
XR_945155.1:n.330+30757C>G
XR_945152.2:n.316+30757C>G
XR_945154.2:n.175-36871C>G
XR_945155.2:n.888+30757C>G
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