Canonical Allele Identifier: CA851031763
Gene:

Linked Data

dbSNP Id: rs1488560242
MyVariant Identifiers: chr8:g.33665931G>A (hg19) chr8:g.33808413G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808413G>A , CM000670.2:g.33808413G>A GRCh38
NC_000008.10:g.33665931G>A , CM000670.1:g.33665931G>A GRCh37
NC_000008.9:g.33785473G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11977G>A
XR_002956701.1:n.240+11977G>A
Search 100 bp 5'
Search 100 bp 3'