Canonical Allele Identifier: CA1223909913
Gene:

Linked Data

dbSNP Id: rs1571984639

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068608A>T , CM000663.2:g.224068608A>T GRCh38
NC_000001.10:g.224256310A>T , CM000663.1:g.224256310A>T GRCh37
NC_000001.9:g.222322933A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+954A>T
XR_001737824.1:n.242+954A>T