Canonical Allele Identifier: CA890013259
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1449955425

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-958T>C NP_001992.1:n.-97-958T>C
NM_002001.4:c.-97-958T>C NP_001992.1:n.-97-958T>C