Canonical Allele Identifier: CA846669386
Gene:

Linked Data

dbSNP Id: rs1208203780
MyVariant Identifiers: chr8:g.123408512A>G (hg19) chr8:g.122396273A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396273A>G , CM000670.2:g.122396273A>G GRCh38
NC_000008.10:g.123408512A>G , CM000670.1:g.123408512A>G GRCh37
NC_000008.9:g.123477693A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2899T>C
XR_928599.3:n.152+2899T>C
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