Canonical Allele Identifier: CA54594658
Gene:

Linked Data

dbSNP Id: rs1048672208
MyVariant Identifiers: chr2:g.119697259T>A (hg19) chr2:g.118939683T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118939683T>A , CM000664.2:g.118939683T>A GRCh38
NC_000002.11:g.119697259T>A , CM000664.1:g.119697259T>A GRCh37
NC_000002.10:g.119413729T>A NCBI36
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