Canonical Allele Identifier: CA890016230
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1336969894
gnomAD v3: 1-159301986-G-T
gnomAD v4: 1-159301986-G-T
MyVariant Identifiers: chr1:g.159271776G>T (hg19) chr1:g.159301986G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301986G>T , CM000663.2:g.159301986G>T GRCh38
NC_000001.10:g.159271776G>T , CM000663.1:g.159271776G>T GRCh37
NC_000001.9:g.157538400G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-320G>T ENSP00000357097.1:n.-59-320G>T
NM_002001.3:c.-59-320G>T NP_001992.1:n.-59-320G>T
NM_002001.4:c.-59-320G>T NP_001992.1:n.-59-320G>T
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