Canonical Allele Identifier: CA890013233

Gene: FCER1A

Linked Data

• dbSNP Id: rs1285533174
• MyVariant Identifiers: chr1:g.159258459del (hg19) ; chr1:g.159288669del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159288670del , CM000663.2:g.159288670del	GRCh38
NC_000001.10:g.159258460del , CM000663.1:g.159258460del	GRCh37
NC_000001.9:g.157525084del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_002001.3:c.-97-1046del	NP_001992.1:n.-97-1046del
NM_002001.4:c.-97-1046del	NP_001992.1:n.-97-1046del