Canonical Allele Identifier: CA909861278
Gene:

Linked Data

dbSNP Id: rs1477002513
MyVariant Identifiers: chr3:g.70626384C>T (hg19) chr3:g.70577233C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577233C>T , CM000665.2:g.70577233C>T GRCh38
NC_000003.11:g.70626384C>T , CM000665.1:g.70626384C>T GRCh37
NC_000003.10:g.70709074C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940947.1:n.407-1280G>A
XR_001740559.1:n.367-1280G>A
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