Canonical Allele Identifier: CA890013232

Gene: FCER1A

Linked Data

• dbSNP Id: rs1314290776
• MyVariant Identifiers: chr1:g.159258451T>A (hg19) ; chr1:g.159288661T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159288661T>A , CM000663.2:g.159288661T>A	GRCh38
NC_000001.10:g.159258451T>A , CM000663.1:g.159258451T>A	GRCh37
NC_000001.9:g.157525075T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_002001.3:c.-97-1055T>A	NP_001992.1:n.-97-1055T>A
NM_002001.4:c.-97-1055T>A	NP_001992.1:n.-97-1055T>A