Canonical Allele Identifier: CA185200379
Gene:

Linked Data

dbSNP Id: rs886193795
MyVariant Identifiers: chr8:g.123407965G>T (hg19) chr8:g.122395726G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395726G>T , CM000670.2:g.122395726G>T GRCh38
NC_000008.10:g.123407965G>T , CM000670.1:g.123407965G>T GRCh37
NC_000008.9:g.123477146G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3446C>A
XR_928599.3:n.152+3446C>A
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