Canonical Allele Identifier: CA343059248
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1255992158

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304113A>G , CM000663.2:g.159304113A>G GRCh38
NC_000001.10:g.159273903A>G , CM000663.1:g.159273903A>G GRCh37
NC_000001.9:g.157540527A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.262A>G MANE Select ENSP00000509626.1:p.Ser88Gly
ENST00000368114.1:c.163A>G ENSP00000357096.1:p.Ser55Gly
ENST00000368115.5:c.262A>G ENSP00000357097.1:p.Ser88Gly
NM_002001.3:c.262A>G NP_001992.1:p.Ser88Gly
NM_001387280.1:c.262A>G MANE Select NP_001374209.1:p.Ser88Gly
NM_001387281.1:c.76+1239A>G NP_001374210.1:n.76+1239A>G
NM_001387282.1:c.163A>G NP_001374211.1:p.Ser55Gly
NM_002001.4:c.262A>G NP_001992.1:p.Ser88Gly