Canonical Allele Identifier: CA175154057
Gene:

Linked Data

dbSNP Id: rs941961866
MyVariant Identifiers: chr8:g.33665930G>C (hg19) chr8:g.33808412G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808412G>C , CM000670.2:g.33808412G>C GRCh38
NC_000008.10:g.33665930G>C , CM000670.1:g.33665930G>C GRCh37
NC_000008.9:g.33785472G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11976G>C
XR_002956701.1:n.240+11976G>C
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