Canonical Allele Identifier: CA1691656442
Gene:

Linked Data

dbSNP Id: rs1803285662

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957848A>T , CM000669.2:g.17957848A>T GRCh38
NC_000007.13:g.17997471A>T , CM000669.1:g.17997471A>T GRCh37
NC_000007.12:g.17963996A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-822A>T