Canonical Allele Identifier: CA1201822902
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288795T= , CM000663.2:g.159288795T= GRCh38
NC_000001.10:g.159258585T= , CM000663.1:g.159258585T= GRCh37
NC_000001.9:g.157525209T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-921T= NP_001992.1:n.-97-921T=
NM_002001.4:c.-97-921T= NP_001992.1:n.-97-921T=