Canonical Allele Identifier: CA1201830654
Gene: FCER1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302049G= , CM000663.2:g.159302049G= GRCh38
NC_000001.10:g.159271839G= , CM000663.1:g.159271839G= GRCh37
NC_000001.9:g.157538463G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-257G= ENSP00000357097.1:n.-59-257G=
NM_002001.3:c.-59-257G= NP_001992.1:n.-59-257G=
NM_002001.4:c.-59-257G= NP_001992.1:n.-59-257G=