Canonical Allele Identifier: CA1201822890
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288763T= , CM000663.2:g.159288763T= GRCh38
NC_000001.10:g.159258553T= , CM000663.1:g.159258553T= GRCh37
NC_000001.9:g.157525177T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002001.3:c.-97-953T= NP_001992.1:n.-97-953T=
NM_002001.4:c.-97-953T= NP_001992.1:n.-97-953T=