Canonical Allele Identifier: CA343057234
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs762504841
gnomAD v3: 1-159302398-T-C
gnomAD v4: 1-159302398-T-C
MyVariant Identifiers: chr1:g.159272188T>C (hg19) chr1:g.159302398T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302398T>C , CM000663.2:g.159302398T>C GRCh38
NC_000001.10:g.159272188T>C , CM000663.1:g.159272188T>C GRCh37
NC_000001.9:g.157538812T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.34T>C MANE Select ENSP00000509626.1:p.Cys12Arg
ENST00000368114.1:c.34T>C ENSP00000357096.1:p.Cys12Arg
ENST00000368115.5:c.34T>C ENSP00000357097.1:p.Cys12Arg
NM_002001.3:c.34T>C NP_001992.1:p.Cys12Arg
NM_001387280.1:c.34T>C MANE Select NP_001374209.1:p.Cys12Arg
NM_001387281.1:c.34T>C NP_001374210.1:p.Cys12Arg
NM_001387282.1:c.34T>C NP_001374211.1:p.Cys12Arg
NM_002001.4:c.34T>C NP_001992.1:p.Cys12Arg
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