Canonical Allele Identifier: CA1201830717
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652448299
gnomAD v4: 1-159302171-GTGGGTAAA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302173_159302180del , CM000663.2:g.159302173_159302180del GRCh38
NC_000001.10:g.159271963_159271970del , CM000663.1:g.159271963_159271970del GRCh37
NC_000001.9:g.157538587_157538594del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-133_-59-126del ENSP00000357097.1:n.-59-133_-59-126del
NM_002001.3:c.-59-133_-59-126del NP_001992.1:n.-59-133_-59-126del
NM_002001.4:c.-59-133_-59-126del NP_001992.1:n.-59-133_-59-126del
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