Canonical Allele Identifier: CA1816081389
Gene:

Linked Data

dbSNP Id: rs1814952434
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122396239C>A , CM000670.2:g.122396239C>A GRCh38
NC_000008.10:g.123408478C>A , CM000670.1:g.123408478C>A GRCh37
NC_000008.9:g.123477659C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928599.1:n.152+2933G>T
XR_928599.3:n.152+2933G>T
Search 100 bp 5'
Search 100 bp 3'