Canonical Allele Identifier: CA1462694177
Gene:

Linked Data

dbSNP Id: rs1756226250

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558042A>T , CM000666.2:g.62558042A>T GRCh38
NC_000004.11:g.63423760A>T , CM000666.1:g.63423760A>T GRCh37
NC_000004.10:g.63106355A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5802A>T