Canonical Allele Identifier: CA343059226
Gene: FCER1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159273899A>C (hg19) chr1:g.159304109A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304109A>C , CM000663.2:g.159304109A>C GRCh38
NC_000001.10:g.159273899A>C , CM000663.1:g.159273899A>C GRCh37
NC_000001.9:g.157540523A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.258A>C MANE Select ENSP00000509626.1:p.Glu86Asp
ENST00000368114.1:c.159A>C ENSP00000357096.1:p.Glu53Asp
ENST00000368115.5:c.258A>C ENSP00000357097.1:p.Glu86Asp
NM_002001.3:c.258A>C NP_001992.1:p.Glu86Asp
NM_001387280.1:c.258A>C MANE Select NP_001374209.1:p.Glu86Asp
NM_001387281.1:c.76+1235A>C NP_001374210.1:n.76+1235A>C
NM_001387282.1:c.159A>C NP_001374211.1:p.Glu53Asp
NM_002001.4:c.258A>C NP_001992.1:p.Glu86Asp
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