Canonical Allele Identifier: CA2157787677
Community Standard Title: NC_000014.9:g.98203821A=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.98203821A= , CM000676.2:g.98203821A= GRCh38
NC_000014.8:g.98670158A= , CM000676.1:g.98670158A= GRCh37
NC_000014.7:g.97739911A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001750875.1:n.1120-654T=