Canonical Allele Identifier: CA2607274678
Gene:

Linked Data

dbSNP Id: rs2102586652

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068575A>G , CM000663.2:g.224068575A>G GRCh38
NC_000001.10:g.224256277A>G , CM000663.1:g.224256277A>G GRCh37
NC_000001.9:g.222322900A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+921A>G
XR_001737824.1:n.242+921A>G