Canonical Allele Identifier: CA890013187
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1440405502
gnomAD v3: 1-159288505-G-A
gnomAD v4: 1-159288505-G-A
MyVariant Identifiers: chr1:g.159258295G>A (hg19) chr1:g.159288505G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159288505G>A , CM000663.2:g.159288505G>A GRCh38
NC_000001.10:g.159258295G>A , CM000663.1:g.159258295G>A GRCh37
NC_000001.9:g.157524919G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_002001.3:c.-97-1211G>A NP_001992.1:n.-97-1211G>A
NM_002001.4:c.-97-1211G>A NP_001992.1:n.-97-1211G>A
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