Canonical Allele Identifier: CA2302316722
Gene:

Linked Data

dbSNP Id: rs1568552050

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645721T>G , CM000680.2:g.49645721T>G GRCh38
NC_000018.9:g.47172091T>G , CM000680.1:g.47172091T>G GRCh37
NC_000018.8:g.45426089T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935461.1:n.162-16313T>G
XR_001753446.1:n.898-16313T>G