Canonical Allele Identifier: CA234906472
Gene:

Linked Data

dbSNP Id: rs11049300
gnomAD v2: 12-28195125-A-G
gnomAD v3: 12-28042192-A-G
gnomAD v4: 12-28042192-A-G
MyVariant Identifiers: chr12:g.28195125A>G (hg19) chr12:g.28042192A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28042192A>G , CM000674.2:g.28042192A>G GRCh38
NC_000012.11:g.28195125A>G , CM000674.1:g.28195125A>G GRCh37
NC_000012.10:g.28086392A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931460.1:n.154-3234T>C
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