Canonical Allele Identifier: CA1161925214
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523573T= , CM000663.2:g.34523573T= GRCh38
NC_000001.10:g.34989174T= , CM000663.1:g.34989174T= GRCh37
NC_000001.9:g.34761761T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947171.1:n.1073+24006A=
XR_001737964.1:n.991+24006A=