Canonical Allele Identifier: CA890016310

Gene: FCER1A

Linked Data

• dbSNP Id: rs1359457224
• MyVariant Identifiers: chr1:g.159272080G>A (hg19) ; chr1:g.159302290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159302290G>A , CM000663.2:g.159302290G>A	GRCh38
NC_000001.10:g.159272080G>A , CM000663.1:g.159272080G>A	GRCh37
NC_000001.9:g.157538704G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368115.5:c.-59-16G>A	ENSP00000357097.1:n.-59-16G>A
NM_002001.3:c.-59-16G>A	NP_001992.1:n.-59-16G>A
NM_002001.4:c.-59-16G>A	NP_001992.1:n.-59-16G>A