Canonical Allele Identifier: CA850516156
Gene:

Linked Data

dbSNP Id: rs1392792658
MyVariant Identifiers: chr8:g.2740513T>C (hg19) chr8:g.2882991T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2882991T>C , CM000670.2:g.2882991T>C GRCh38
NC_000008.10:g.2740513T>C , CM000670.1:g.2740513T>C GRCh37
NC_000008.9:g.2727920T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941367.1:n.212-42774T>C
NR_168441.1:n.1166+45227T>C
NR_168442.1:n.1331-33344T>C
NR_168443.1:n.1171+45227T>C
NR_168444.1:n.1166+45227T>C
NR_168445.1:n.1249+45144T>C
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