Canonical Allele Identifier: CA850516160
Gene:

Linked Data

dbSNP Id: rs1323120893
MyVariant Identifiers: chr8:g.2740514G>A (hg19) chr8:g.2882992G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2882992G>A , CM000670.2:g.2882992G>A GRCh38
NC_000008.10:g.2740514G>A , CM000670.1:g.2740514G>A GRCh37
NC_000008.9:g.2727921G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941367.1:n.212-42773G>A
NR_168441.1:n.1166+45228G>A
NR_168442.1:n.1331-33343G>A
NR_168443.1:n.1171+45228G>A
NR_168444.1:n.1166+45228G>A
NR_168445.1:n.1249+45145G>A
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