Canonical Allele Identifier: CA1201822799
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288648T= , CM000663.2:g.159288648T= GRCh38
NC_000001.10:g.159258438T= , CM000663.1:g.159258438T= GRCh37
NC_000001.9:g.157525062T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1068T= NP_001992.1:n.-97-1068T=
NM_002001.4:c.-97-1068T= NP_001992.1:n.-97-1068T=