Canonical Allele Identifier: CA1223909912
Gene:

Linked Data

dbSNP Id: rs1571984639

Genomic Alleles

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

Transcript Alleles

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