Canonical Allele Identifier: CA1369169793
Gene:

Linked Data

dbSNP Id: rs2041752342

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.61427945G>A , CM000665.2:g.61427945G>A GRCh38
NC_000003.11:g.61413619G>A , CM000665.1:g.61413619G>A GRCh37
NC_000003.10:g.61388659G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940892.1:n.165-259C>T
XR_940893.1:n.164+569C>T
XR_001740725.1:n.202+569C>T
XR_940892.2:n.203-259C>T