Canonical Allele Identifier: CA890013269
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1217811882

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288776C>G , CM000663.2:g.159288776C>G GRCh38
NC_000001.10:g.159258566C>G , CM000663.1:g.159258566C>G GRCh37
NC_000001.9:g.157525190C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-940C>G NP_001992.1:n.-97-940C>G
NM_002001.4:c.-97-940C>G NP_001992.1:n.-97-940C>G