Canonical Allele Identifier: CA1187952

Gene: FCER1A

Linked Data

• dbSNP Id: rs764081099
• ExAC: 1:159273896 T / G
• gnomAD v2: 1-159273896-T-G
• MyVariant Identifiers: chr1:g.159273896T>G (hg19) ; chr1:g.159304106T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159304106T>G , CM000663.2:g.159304106T>G	GRCh38
NC_000001.10:g.159273896T>G , CM000663.1:g.159273896T>G	GRCh37
NC_000001.9:g.157540520T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000693622.1:c.255T>G MANE Select	ENSP00000509626.1:p.Phe85Leu
ENST00000368114.1:c.156T>G	ENSP00000357096.1:p.Phe52Leu
ENST00000368115.5:c.255T>G	ENSP00000357097.1:p.Phe85Leu
NM_002001.3:c.255T>G	NP_001992.1:p.Phe85Leu
NM_001387280.1:c.255T>G MANE Select	NP_001374209.1:p.Phe85Leu
NM_001387281.1:c.76+1232T>G	NP_001374210.1:n.76+1232T>G
NM_001387282.1:c.156T>G	NP_001374211.1:p.Phe52Leu
NM_002001.4:c.255T>G	NP_001992.1:p.Phe85Leu