Canonical Allele Identifier: CA1187953
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs375885500

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.258A>G MANE Select ENSP00000509626.1:p.Glu86=
ENST00000368114.1:c.159A>G ENSP00000357096.1:p.Glu53=
ENST00000368115.5:c.258A>G ENSP00000357097.1:p.Glu86=
NM_002001.3:c.258A>G NP_001992.1:p.Glu86=
NM_001387280.1:c.258A>G MANE Select NP_001374209.1:p.Glu86=
NM_001387281.1:c.76+1235A>G NP_001374210.1:n.76+1235A>G
NM_001387282.1:c.159A>G NP_001374211.1:p.Glu53=
NM_002001.4:c.258A>G NP_001992.1:p.Glu86=