Canonical Allele Identifier: CA1201822886
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288758T= , CM000663.2:g.159288758T= GRCh38
NC_000001.10:g.159258548T= , CM000663.1:g.159258548T= GRCh37
NC_000001.9:g.157525172T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002001.3:c.-97-958T= NP_001992.1:n.-97-958T=
NM_002001.4:c.-97-958T= NP_001992.1:n.-97-958T=