Canonical Allele Identifier: CA526574156

Gene: FCER1A

Linked Data

• dbSNP Id: rs1239411837
• gnomAD v2: 1-159258553-T-G
• gnomAD v3: 1-159288763-T-G
• gnomAD v4: 1-159288763-T-G
• MyVariant Identifiers: chr1:g.159258553T>G (hg19) ; chr1:g.159288763T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159288763T>G , CM000663.2:g.159288763T>G	GRCh38
NC_000001.10:g.159258553T>G , CM000663.1:g.159258553T>G	GRCh37
NC_000001.9:g.157525177T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_002001.3:c.-97-953T>G	NP_001992.1:n.-97-953T>G
NM_002001.4:c.-97-953T>G	NP_001992.1:n.-97-953T>G