Canonical Allele Identifier: CA181547502
Gene:

Linked Data

dbSNP Id: rs909385128
MyVariant Identifiers: chr8:g.89547971A>G (hg19) chr8:g.88535742A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535742A>G , CM000670.2:g.88535742A>G GRCh38
NC_000008.10:g.89547971A>G , CM000670.1:g.89547971A>G GRCh37
NC_000008.9:g.89617087A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10775T>C
XR_001745653.2:n.286-6938A>G
XR_928383.3:n.1475+10775T>C
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