Canonical Allele Identifier: CA343059254
Gene: FCER1A HGNC NCBI

Linked Data

gnomAD v4: 1-159304114-G-A
MyVariant Identifiers: chr1:g.159273904G>A (hg19) chr1:g.159304114G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304114G>A , CM000663.2:g.159304114G>A GRCh38
NC_000001.10:g.159273904G>A , CM000663.1:g.159273904G>A GRCh37
NC_000001.9:g.157540528G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.263G>A MANE Select ENSP00000509626.1:p.Ser88Asn
ENST00000368114.1:c.164G>A ENSP00000357096.1:p.Ser55Asn
ENST00000368115.5:c.263G>A ENSP00000357097.1:p.Ser88Asn
NM_002001.3:c.263G>A NP_001992.1:p.Ser88Asn
NM_001387280.1:c.263G>A MANE Select NP_001374209.1:p.Ser88Asn
NM_001387281.1:c.76+1240G>A NP_001374210.1:n.76+1240G>A
NM_001387282.1:c.164G>A NP_001374211.1:p.Ser55Asn
NM_002001.4:c.263G>A NP_001992.1:p.Ser88Asn
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