Canonical Allele Identifier: CA1356887154
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.34921342T= , CM000665.2:g.34921342T= GRCh38
NC_000003.11:g.34962834T= , CM000665.1:g.34962834T= GRCh37
NC_000003.10:g.34937838T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110817.1:n.207-41876A=