Canonical Allele Identifier: CA2156233153
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94944195T= , CM000676.2:g.94944195T= GRCh38
NC_000014.8:g.95410532T= , CM000676.1:g.95410532T= GRCh37
NC_000014.7:g.94480285T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001750935.1:n.500-266A=