Canonical Allele Identifier: CA890013279
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1442421247

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288825C>T , CM000663.2:g.159288825C>T GRCh38
NC_000001.10:g.159258615C>T , CM000663.1:g.159258615C>T GRCh37
NC_000001.9:g.157525239C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-891C>T NP_001992.1:n.-97-891C>T
NM_002001.4:c.-97-891C>T NP_001992.1:n.-97-891C>T