Canonical Allele Identifier: CA13689962
Gene:

Linked Data

dbSNP Id: rs1179246
gnomAD v2: 12-68640583-A-C
gnomAD v3: 12-68246803-A-C
gnomAD v4: 12-68246803-A-C
MyVariant Identifiers: chr12:g.68640583A>C (hg19) chr12:g.68246803A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68246803A>C , CM000674.2:g.68246803A>C GRCh38
NC_000012.11:g.68640583A>C , CM000674.1:g.68640583A>C GRCh37
NC_000012.10:g.66926850A>C NCBI36
NG_060763.1:g.11802T>G

Transcript Alleles

HGVS Amino-acid change
XR_945055.1:n.265-17855A>C
XR_002957418.1:n.281-17855A>C
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