Canonical Allele Identifier: CA2193585443
Gene:

Linked Data

dbSNP Id: rs2082249141
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152198C>T , CM000677.2:g.87152198C>T GRCh38
NC_000015.9:g.87695429C>T , CM000677.1:g.87695429C>T GRCh37
NC_000015.8:g.85496433C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26029C>T
XR_932582.2:n.167-26029C>T
Search 100 bp 5'
Search 100 bp 3'