Canonical Allele Identifier: CA343059234
Gene: FCER1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159273900G>C (hg19) chr1:g.159304110G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304110G>C , CM000663.2:g.159304110G>C GRCh38
NC_000001.10:g.159273900G>C , CM000663.1:g.159273900G>C GRCh37
NC_000001.9:g.157540524G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.259G>C MANE Select ENSP00000509626.1:p.Asp87His
ENST00000368114.1:c.160G>C ENSP00000357096.1:p.Asp54His
ENST00000368115.5:c.259G>C ENSP00000357097.1:p.Asp87His
NM_002001.3:c.259G>C NP_001992.1:p.Asp87His
NM_001387280.1:c.259G>C MANE Select NP_001374209.1:p.Asp87His
NM_001387281.1:c.76+1236G>C NP_001374210.1:n.76+1236G>C
NM_001387282.1:c.160G>C NP_001374211.1:p.Asp54His
NM_002001.4:c.259G>C NP_001992.1:p.Asp87His
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