Canonical Allele Identifier: CA799753666
Gene:

Linked Data

dbSNP Id: rs1178095238
MyVariant Identifiers: chr4:g.90577167G>A (hg19) chr4:g.89656016G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89656016G>A , CM000666.2:g.89656016G>A GRCh38
NC_000004.11:g.90577167G>A , CM000666.1:g.90577167G>A GRCh37
NC_000004.10:g.90796190G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+28099G>A
XR_938987.1:n.688+28099G>A
XR_938988.1:n.554+28099G>A
XR_938990.1:n.299-35269G>A
XR_938991.1:n.434+28099G>A
XR_938994.1:n.779+28099G>A
XR_938995.1:n.613+28099G>A
XR_938986.2:n.459+28099G>A
XR_938987.2:n.748+28099G>A
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