Canonical Allele Identifier: CA2695601301
Gene:

Linked Data

dbSNP Id: rs2124127347

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523688G>A , CM000663.2:g.34523688G>A GRCh38
NC_000001.10:g.34989289G>A , CM000663.1:g.34989289G>A GRCh37
NC_000001.9:g.34761876G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23891C>T
XR_001737964.1:n.991+23891C>T