Canonical Allele Identifier: CA799753582
Gene:

Linked Data

dbSNP Id: rs1178022551
MyVariant Identifiers: chr4:g.90577055T>C (hg19) chr4:g.89655904T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655904T>C , CM000666.2:g.89655904T>C GRCh38
NC_000004.11:g.90577055T>C , CM000666.1:g.90577055T>C GRCh37
NC_000004.10:g.90796078T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27987T>C
XR_938987.1:n.688+27987T>C
XR_938988.1:n.554+27987T>C
XR_938990.1:n.299-35381T>C
XR_938991.1:n.434+27987T>C
XR_938994.1:n.779+27987T>C
XR_938995.1:n.613+27987T>C
XR_938986.2:n.459+27987T>C
XR_938987.2:n.748+27987T>C
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