Canonical Allele Identifier: CA1889344534
Gene:

Linked Data

dbSNP Id: rs1832130470

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697603A>G , CM000672.2:g.8697603A>G GRCh38
NC_000010.10:g.8739566A>G , CM000672.1:g.8739566A>G GRCh37
NC_000010.9:g.8779572A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27802T>C