Canonical Allele Identifier: CA1012755375
Gene:

Linked Data

dbSNP Id: rs1655906282

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068502A>G , CM000663.2:g.224068502A>G GRCh38
NC_000001.10:g.224256204A>G , CM000663.1:g.224256204A>G GRCh37
NC_000001.9:g.222322827A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949173.1:n.385+848A>G
XR_001737824.1:n.242+848A>G