Canonical Allele Identifier: CA526574148

Gene: FCER1A

Linked Data

• dbSNP Id: rs1318652128
• gnomAD v2: 1-159258535-C-T
• gnomAD v3: 1-159288745-C-T
• gnomAD v4: 1-159288745-C-T
• MyVariant Identifiers: chr1:g.159258535C>T (hg19) ; chr1:g.159288745C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159288745C>T , CM000663.2:g.159288745C>T	GRCh38
NC_000001.10:g.159258535C>T , CM000663.1:g.159258535C>T	GRCh37
NC_000001.9:g.157525159C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_002001.3:c.-97-971C>T	NP_001992.1:n.-97-971C>T
NM_002001.4:c.-97-971C>T	NP_001992.1:n.-97-971C>T