Canonical Allele Identifier: CA1139854055
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.94564065C= , CM000663.2:g.94564065C= GRCh38
NC_000001.10:g.95029621C= , CM000663.1:g.95029621C= GRCh37
NC_000001.9:g.94802209C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738161.1:n.461+452C=