Canonical Allele Identifier: CA890013218
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1471511072
gnomAD v3: 1-159288611-T-C
gnomAD v4: 1-159288611-T-C
MyVariant Identifiers: chr1:g.159258401T>C (hg19) chr1:g.159288611T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288611T>C , CM000663.2:g.159288611T>C GRCh38
NC_000001.10:g.159258401T>C , CM000663.1:g.159258401T>C GRCh37
NC_000001.9:g.157525025T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_002001.3:c.-97-1105T>C NP_001992.1:n.-97-1105T>C
NM_002001.4:c.-97-1105T>C NP_001992.1:n.-97-1105T>C
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