Canonical Allele Identifier: CA1691656436
Gene:

Linked Data

dbSNP Id: rs1583893688

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.17957835A>T , CM000669.2:g.17957835A>T GRCh38
NC_000007.13:g.17997458A>T , CM000669.1:g.17997458A>T GRCh37
NC_000007.12:g.17963983A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927078.1:n.271-835A>T