Canonical Allele Identifier: CA893195895
Gene:

Linked Data

dbSNP Id: rs1199674570
MyVariant Identifiers: chr2:g.773338T>C (hg19) chr2:g.773338T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.773338T>C , CM000664.2:g.773338T>C GRCh38
NC_000002.11:g.773338T>C , CM000664.1:g.773338T>C GRCh37
NC_000002.10:g.763338T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510439.1:c.-24-3498T>C XP_011508741.1:n.-24-3498T>C
XM_011510440.1:c.-24-3498T>C XP_011508742.1:n.-24-3498T>C
XM_011510441.1:c.-24-3498T>C XP_011508743.1:n.-24-3498T>C
XM_011510442.1:c.-24-3498T>C XP_011508744.1:n.-24-3498T>C
XM_011510443.1:c.-24-3498T>C XP_011508745.1:n.-24-3498T>C
XR_922708.1:n.4001-3498T>C
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