Canonical Allele Identifier: CA1223909904
Gene:

Linked Data

dbSNP Id: rs1655906997

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068588A>T , CM000663.2:g.224068588A>T GRCh38
NC_000001.10:g.224256290A>T , CM000663.1:g.224256290A>T GRCh37
NC_000001.9:g.222322913A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+934A>T
XR_001737824.1:n.242+934A>T