Canonical Allele Identifier: CA1008275941
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652446728
gnomAD v3: 1-159302114-CCT-C
gnomAD v4: 1-159302114-CCT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302122_159302123del , CM000663.2:g.159302122_159302123del GRCh38
NC_000001.10:g.159271912_159271913del , CM000663.1:g.159271912_159271913del GRCh37
NC_000001.9:g.157538536_157538537del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-184_-59-183del ENSP00000357097.1:n.-59-184_-59-183del
NM_002001.3:c.-59-184_-59-183del NP_001992.1:n.-59-184_-59-183del
NM_002001.4:c.-59-184_-59-183del NP_001992.1:n.-59-184_-59-183del
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