Canonical Allele Identifier: CA845291758
Gene:

Linked Data

dbSNP Id: rs1336727574
MyVariant Identifiers: chr8:g.108789774A>G (hg19) chr8:g.107777546A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.107777546A>G , CM000670.2:g.107777546A>G GRCh38
NC_000008.10:g.108789774A>G , CM000670.1:g.108789774A>G GRCh37
NC_000008.9:g.108858950A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928527.1:n.185+930T>C
XR_928527.2:n.219+930T>C
Search 100 bp 5'
Search 100 bp 3'