Canonical Allele Identifier: CA989591462
Gene:

Linked Data

dbSNP Id: rs1910117795

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477619A>G , CM000680.2:g.41477619A>G GRCh38
NC_000018.9:g.39057583A>G , CM000680.1:g.39057583A>G GRCh37
NC_000018.8:g.37311581A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26515A>G