Canonical Allele Identifier: CA1201822814
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652076547

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288663T>G , CM000663.2:g.159288663T>G GRCh38
NC_000001.10:g.159258453T>G , CM000663.1:g.159258453T>G GRCh37
NC_000001.9:g.157525077T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002001.3:c.-97-1053T>G NP_001992.1:n.-97-1053T>G
NM_002001.4:c.-97-1053T>G NP_001992.1:n.-97-1053T>G