Canonical Allele Identifier: CA421593214

Gene: FCER1A

Linked Data

• dbSNP Id: rs1652525792
• gnomAD v3: 1-159304112-C-T
• gnomAD v4: 1-159304112-C-T
• MyVariant Identifiers: chr1:g.159273902C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159304112C>T , CM000663.2:g.159304112C>T	GRCh38
NC_000001.10:g.159273902C>T , CM000663.1:g.159273902C>T	GRCh37
NC_000001.9:g.157540526C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693622.1:c.261C>T MANE Select	ENSP00000509626.1:p.Asp87=
ENST00000368114.1:c.162C>T	ENSP00000357096.1:p.Asp54=
ENST00000368115.5:c.261C>T	ENSP00000357097.1:p.Asp87=
NM_002001.3:c.261C>T	NP_001992.1:p.Asp87=
NM_001387280.1:c.261C>T MANE Select	NP_001374209.1:p.Asp87=
NM_001387281.1:c.76+1238C>T	NP_001374210.1:n.76+1238C>T
NM_001387282.1:c.162C>T	NP_001374211.1:p.Asp54=
NM_002001.4:c.261C>T	NP_001992.1:p.Asp87=