Canonical Allele Identifier: CA1201830691
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302119C= , CM000663.2:g.159302119C= GRCh38
NC_000001.10:g.159271909C= , CM000663.1:g.159271909C= GRCh37
NC_000001.9:g.157538533C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-187C= ENSP00000357097.1:n.-59-187C=
NM_002001.3:c.-59-187C= NP_001992.1:n.-59-187C=
NM_002001.4:c.-59-187C= NP_001992.1:n.-59-187C=