Canonical Allele Identifier: CA185200431
Gene:

Linked Data

dbSNP Id: rs907517419
MyVariant Identifiers: chr8:g.123408327A>G (hg19) chr8:g.122396088A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396088A>G , CM000670.2:g.122396088A>G GRCh38
NC_000008.10:g.123408327A>G , CM000670.1:g.123408327A>G GRCh37
NC_000008.9:g.123477508A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3084T>C
XR_928599.3:n.152+3084T>C
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