Canonical Allele Identifier: CA2697468500
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs2102227950

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302031A>T , CM000663.2:g.159302031A>T GRCh38
NC_000001.10:g.159271821A>T , CM000663.1:g.159271821A>T GRCh37
NC_000001.9:g.157538445A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-275A>T ENSP00000357097.1:n.-59-275A>T
NM_002001.3:c.-59-275A>T NP_001992.1:n.-59-275A>T
NM_002001.4:c.-59-275A>T NP_001992.1:n.-59-275A>T