Canonical Allele Identifier: CA526577031
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1229602700
gnomAD v2: 1-159271909-C-G
gnomAD v3: 1-159302119-C-G
gnomAD v4: 1-159302119-C-G
MyVariant Identifiers: chr1:g.159271909C>G (hg19) chr1:g.159302119C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302119C>G , CM000663.2:g.159302119C>G GRCh38
NC_000001.10:g.159271909C>G , CM000663.1:g.159271909C>G GRCh37
NC_000001.9:g.157538533C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-187C>G ENSP00000357097.1:n.-59-187C>G
NM_002001.3:c.-59-187C>G NP_001992.1:n.-59-187C>G
NM_002001.4:c.-59-187C>G NP_001992.1:n.-59-187C>G
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