Canonical Allele Identifier: CA343059204
Gene: FCER1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.159273895T>A (hg19) chr1:g.159304105T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159304105T>A , CM000663.2:g.159304105T>A GRCh38
NC_000001.10:g.159273895T>A , CM000663.1:g.159273895T>A GRCh37
NC_000001.9:g.157540519T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693622.1:c.254T>A MANE Select ENSP00000509626.1:p.Phe85Tyr
ENST00000368114.1:c.155T>A ENSP00000357096.1:p.Phe52Tyr
ENST00000368115.5:c.254T>A ENSP00000357097.1:p.Phe85Tyr
NM_002001.3:c.254T>A NP_001992.1:p.Phe85Tyr
NM_001387280.1:c.254T>A MANE Select NP_001374209.1:p.Phe85Tyr
NM_001387281.1:c.76+1231T>A NP_001374210.1:n.76+1231T>A
NM_001387282.1:c.155T>A NP_001374211.1:p.Phe52Tyr
NM_002001.4:c.254T>A NP_001992.1:p.Phe85Tyr
Search 100 bp 5'
Search 100 bp 3'