Canonical Allele Identifier: CA421317757
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1266749815
gnomAD v3: 1-159302391-T-A
gnomAD v4: 1-159302391-T-A
MyVariant Identifiers: chr1:g.159272181T>A (hg19) chr1:g.159302391T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302391T>A , CM000663.2:g.159302391T>A GRCh38
NC_000001.10:g.159272181T>A , CM000663.1:g.159272181T>A GRCh37
NC_000001.9:g.157538805T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000693622.1:c.27T>A MANE Select ENSP00000509626.1:p.Thr9=
ENST00000368114.1:c.27T>A ENSP00000357096.1:p.Thr9=
ENST00000368115.5:c.27T>A ENSP00000357097.1:p.Thr9=
NM_002001.3:c.27T>A NP_001992.1:p.Thr9=
NM_001387280.1:c.27T>A MANE Select NP_001374209.1:p.Thr9=
NM_001387281.1:c.27T>A NP_001374210.1:p.Thr9=
NM_001387282.1:c.27T>A NP_001374211.1:p.Thr9=
NM_002001.4:c.27T>A NP_001992.1:p.Thr9=
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