Canonical Allele Identifier: CA1201830687
Gene: FCER1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302114_159302116delinsCCT , CM000663.2:g.159302114_159302116delinsCCT GRCh38
NC_000001.10:g.159271904_159271906delinsCCT , CM000663.1:g.159271904_159271906delinsCCT GRCh37
NC_000001.9:g.157538528_157538530delinsCCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-192_-59-190delinsCCT ENSP00000357097.1:n.-59-192_-59-190delinsCCT
NM_002001.3:c.-59-192_-59-190delinsCCT NP_001992.1:n.-59-192_-59-190delinsCCT
NM_002001.4:c.-59-192_-59-190delinsCCT NP_001992.1:n.-59-192_-59-190delinsCCT
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