Canonical Allele Identifier: CA1804794316
Gene:

Linked Data

dbSNP Id: rs1810399690
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269712C>A , CM000670.2:g.97269712C>A GRCh38
NC_000008.10:g.98281940C>A , CM000670.1:g.98281940C>A GRCh37
NC_000008.9:g.98351116C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149358G>T
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Search 100 bp 3'