Canonical Allele Identifier: CA239298379
Gene:

Linked Data

dbSNP Id: rs900916530
MyVariant Identifiers: chr12:g.76398683A>G (hg19) chr12:g.76004903A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.76004903A>G , CM000674.2:g.76004903A>G GRCh38
NC_000012.11:g.76398683A>G , CM000674.1:g.76398683A>G GRCh37
NC_000012.10:g.74684950A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945110.1:n.311+1286T>C
XR_001749218.2:n.402+1286T>C
XR_945110.3:n.402+1286T>C
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