Canonical Allele Identifier: CA421593038
Gene: FCER1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159273794T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304004T>C , CM000663.2:g.159304004T>C GRCh38
NC_000001.10:g.159273794T>C , CM000663.1:g.159273794T>C GRCh37
NC_000001.9:g.157540418T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693622.1:c.153T>C MANE Select ENSP00000509626.1:p.Cys51=
ENST00000368114.1:c.77-23T>C ENSP00000357096.1:n.77-23T>C
ENST00000368115.5:c.153T>C ENSP00000357097.1:p.Cys51=
NM_002001.3:c.153T>C NP_001992.1:p.Cys51=
NM_001387280.1:c.153T>C MANE Select NP_001374209.1:p.Cys51=
NM_001387281.1:c.76+1130T>C NP_001374210.1:n.76+1130T>C
NM_001387282.1:c.77-23T>C NP_001374211.1:n.77-23T>C
NM_002001.4:c.153T>C NP_001992.1:p.Cys51=
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