Canonical Allele Identifier: CA47693372
Gene:

Linked Data

dbSNP Id: rs993779902
MyVariant Identifiers: chr2:g.52949622A>G (hg19) chr2:g.52722484A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722484A>G , CM000664.2:g.52722484A>G GRCh38
NC_000002.11:g.52949622A>G , CM000664.1:g.52949622A>G GRCh37
NC_000002.10:g.52803126A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.773T>C
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