Canonical Allele Identifier: CA846669082
Gene:

Linked Data

dbSNP Id: rs1329288252
MyVariant Identifiers: chr8:g.123407948T>C (hg19) chr8:g.122395709T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122395709T>C , CM000670.2:g.122395709T>C GRCh38
NC_000008.10:g.123407948T>C , CM000670.1:g.123407948T>C GRCh37
NC_000008.9:g.123477129T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3463A>G
XR_928599.3:n.152+3463A>G
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Search 100 bp 3'