Canonical Allele Identifier: CA846669271
Gene:

Linked Data

dbSNP Id: rs1337559071
MyVariant Identifiers: chr8:g.123408328T>C (hg19) chr8:g.122396089T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396089T>C , CM000670.2:g.122396089T>C GRCh38
NC_000008.10:g.123408328T>C , CM000670.1:g.123408328T>C GRCh37
NC_000008.9:g.123477509T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+3083A>G
XR_928599.3:n.152+3083A>G
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