Canonical Allele Identifier: CA890013238

Gene: FCER1A

Linked Data

• dbSNP Id: rs1276143833
• gnomAD v3: 1-159288691-T-G
• gnomAD v4: 1-159288691-T-G
• MyVariant Identifiers: chr1:g.159258481T>G (hg19) ; chr1:g.159288691T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159288691T>G , CM000663.2:g.159288691T>G	GRCh38
NC_000001.10:g.159258481T>G , CM000663.1:g.159258481T>G	GRCh37
NC_000001.9:g.157525105T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_002001.3:c.-97-1025T>G	NP_001992.1:n.-97-1025T>G
NM_002001.4:c.-97-1025T>G	NP_001992.1:n.-97-1025T>G