Canonical Allele Identifier: CA73191357
Gene:

Linked Data

dbSNP Id: rs760723079
MyVariant Identifiers: chr3:g.34962837A>G (hg19) chr3:g.34921345A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.34921345A>G , CM000665.2:g.34921345A>G GRCh38
NC_000003.11:g.34962837A>G , CM000665.1:g.34962837A>G GRCh37
NC_000003.10:g.34937841A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110817.1:n.207-41879T>C
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