Canonical Allele Identifier: CA799758196
Gene:

Linked Data

dbSNP Id: rs1339963636
MyVariant Identifiers: chr4:g.90519027T>C (hg19) chr4:g.89597876T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597876T>C , CM000666.2:g.89597876T>C GRCh38
NC_000004.11:g.90519027T>C , CM000666.1:g.90519027T>C GRCh37
NC_000004.10:g.90738050T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+9936T>C
XR_938987.1:n.433-277T>C
XR_938988.1:n.299-277T>C
XR_938990.1:n.298+9936T>C
XR_938991.1:n.298+9936T>C
XR_938992.1:n.298+9936T>C
XR_938994.1:n.643+9936T>C
XR_938995.1:n.477+9936T>C
XR_938996.1:n.298+9936T>C
XR_938997.1:n.298+9936T>C
XR_938986.2:n.323+9936T>C
XR_938987.2:n.493-277T>C
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