Canonical Allele Identifier: CA1818149935
Gene:

Linked Data

dbSNP Id: rs1711686

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999792G>A , CM000670.2:g.126999792G>A GRCh38
NC_000008.10:g.128012037G>A , CM000670.1:g.128012037G>A GRCh37
NC_000008.9:g.128081219G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1301-6763G>A