Canonical Allele Identifier: CA31357293

Gene: FCER1A

Linked Data

• dbSNP Id: rs181213318
• gnomAD v2: 1-159258500-G-T
• gnomAD v3: 1-159288710-G-T
• gnomAD v4: 1-159288710-G-T
• MyVariant Identifiers: chr1:g.159258500G>T (hg19) ; chr1:g.159288710G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159288710G>T , CM000663.2:g.159288710G>T	GRCh38
NC_000001.10:g.159258500G>T , CM000663.1:g.159258500G>T	GRCh37
NC_000001.9:g.157525124G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_002001.3:c.-97-1006G>T	NP_001992.1:n.-97-1006G>T
NM_002001.4:c.-97-1006G>T	NP_001992.1:n.-97-1006G>T