Canonical Allele Identifier: CA1008275913
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652443478
gnomAD v3: 1-159302003-G-T
gnomAD v4: 1-159302003-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302003G>T , CM000663.2:g.159302003G>T GRCh38
NC_000001.10:g.159271793G>T , CM000663.1:g.159271793G>T GRCh37
NC_000001.9:g.157538417G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000368115.5:c.-59-303G>T ENSP00000357097.1:n.-59-303G>T
NM_002001.3:c.-59-303G>T NP_001992.1:n.-59-303G>T
NM_002001.4:c.-59-303G>T NP_001992.1:n.-59-303G>T
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