Canonical Allele Identifier: CA890016185
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1344562633
gnomAD v3: 1-159301885-G-C
gnomAD v4: 1-159301885-G-C
MyVariant Identifiers: chr1:g.159271675G>C (hg19) chr1:g.159301885G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159301885G>C , CM000663.2:g.159301885G>C GRCh38
NC_000001.10:g.159271675G>C , CM000663.1:g.159271675G>C GRCh37
NC_000001.9:g.157538299G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-421G>C ENSP00000357097.1:n.-59-421G>C
NM_002001.3:c.-59-421G>C NP_001992.1:n.-59-421G>C
NM_002001.4:c.-59-421G>C NP_001992.1:n.-59-421G>C
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