Canonical Allele Identifier: CA2156233165
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.94944223T= , CM000676.2:g.94944223T= GRCh38
NC_000014.8:g.95410560T= , CM000676.1:g.95410560T= GRCh37
NC_000014.7:g.94480313T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001750935.1:n.500-294A=