Canonical Allele Identifier: CA526577022

Gene: FCER1A

Linked Data

• dbSNP Id: rs1461390679
• gnomAD v2: 1-159271785-A-G
• gnomAD v3: 1-159301995-A-G
• gnomAD v4: 1-159301995-A-G
• MyVariant Identifiers: chr1:g.159271785A>G (hg19) ; chr1:g.159301995A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159301995A>G , CM000663.2:g.159301995A>G	GRCh38
NC_000001.10:g.159271785A>G , CM000663.1:g.159271785A>G	GRCh37
NC_000001.9:g.157538409A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368115.5:c.-59-311A>G	ENSP00000357097.1:n.-59-311A>G
NM_002001.3:c.-59-311A>G	NP_001992.1:n.-59-311A>G
NM_002001.4:c.-59-311A>G	NP_001992.1:n.-59-311A>G