Canonical Allele Identifier: CA1769199492
Gene:

Linked Data

dbSNP Id: rs1585177258

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130166A>G , CM000670.2:g.20130166A>G GRCh38
NC_000008.10:g.19987677A>G , CM000670.1:g.19987677A>G GRCh37
NC_000008.9:g.20031957A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+247A>G
XR_949563.2:n.3400+247A>G