Canonical Allele Identifier: CA851031693
Gene:

Linked Data

dbSNP Id: rs1370657875
MyVariant Identifiers: chr8:g.33665748A>C (hg19) chr8:g.33808230A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808230A>C , CM000670.2:g.33808230A>C GRCh38
NC_000008.10:g.33665748A>C , CM000670.1:g.33665748A>C GRCh37
NC_000008.9:g.33785290A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949659.1:n.240+11794A>C
XR_002956701.1:n.240+11794A>C
Search 100 bp 5'
Search 100 bp 3'