Canonical Allele Identifier: CA778454209
Gene:

Linked Data

dbSNP Id: rs1239524175

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756654A>T , CM000680.2:g.31756654A>T GRCh38
NC_000018.9:g.29336617A>T , CM000680.1:g.29336617A>T GRCh37
NC_000018.8:g.27590615A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5485A>T