Canonical Allele Identifier: CA2302316785
Gene:

Linked Data

dbSNP Id: rs2021993040

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.49645846G>T , CM000680.2:g.49645846G>T GRCh38
NC_000018.9:g.47172216G>T , CM000680.1:g.47172216G>T GRCh37
NC_000018.8:g.45426214G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935461.1:n.162-16188G>T
XR_001753446.1:n.898-16188G>T