Canonical Allele Identifier: CA10767831
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523636G>A , CM000663.2:g.34523636G>A GRCh38
NC_000001.10:g.34989237G>A , CM000663.1:g.34989237G>A GRCh37
NC_000001.9:g.34761824G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+23943C>T
XR_001737964.1:n.991+23943C>T