Canonical Allele Identifier: CA1008270687
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652074900

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288602G>T , CM000663.2:g.159288602G>T GRCh38
NC_000001.10:g.159258392G>T , CM000663.1:g.159258392G>T GRCh37
NC_000001.9:g.157525016G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1114G>T NP_001992.1:n.-97-1114G>T
NM_002001.4:c.-97-1114G>T NP_001992.1:n.-97-1114G>T