Canonical Allele Identifier: CA2386425967
Gene:

Linked Data

dbSNP Id: rs2045226011

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.32890418G>A , CM000683.2:g.32890418G>A GRCh38
NC_000021.8:g.34262726G>A , CM000683.1:g.34262726G>A GRCh37
NC_000021.7:g.33184596G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937669.1:n.460-3160G>A
XR_937669.2:n.1038-3160G>A