Canonical Allele Identifier: CA890016219
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1283744643
MyVariant Identifiers: chr1:g.159271757del (hg19) chr1:g.159301967del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301968del , CM000663.2:g.159301968del GRCh38
NC_000001.10:g.159271758del , CM000663.1:g.159271758del GRCh37
NC_000001.9:g.157538382del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-338del ENSP00000357097.1:n.-59-338del
NM_002001.3:c.-59-338del NP_001992.1:n.-59-338del
NM_002001.4:c.-59-338del NP_001992.1:n.-59-338del
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