Canonical Allele Identifier: CA799758238
Gene:

Linked Data

dbSNP Id: rs1291694134
MyVariant Identifiers: chr4:g.90519083C>A (hg19) chr4:g.89597932C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597932C>A , CM000666.2:g.89597932C>A GRCh38
NC_000004.11:g.90519083C>A , CM000666.1:g.90519083C>A GRCh37
NC_000004.10:g.90738106C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+9992C>A
XR_938987.1:n.433-221C>A
XR_938988.1:n.299-221C>A
XR_938990.1:n.298+9992C>A
XR_938991.1:n.298+9992C>A
XR_938992.1:n.298+9992C>A
XR_938994.1:n.643+9992C>A
XR_938995.1:n.477+9992C>A
XR_938996.1:n.298+9992C>A
XR_938997.1:n.298+9992C>A
XR_938986.2:n.323+9992C>A
XR_938987.2:n.493-221C>A
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