Canonical Allele Identifier: CA2284269279
Gene:

Linked Data

dbSNP Id: rs1969408387

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10382820T>A , CM000680.2:g.10382820T>A GRCh38
NC_000018.9:g.10382817T>A , CM000680.1:g.10382817T>A GRCh37
NC_000018.8:g.10372817T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935143.1:n.919+1467T>A