Canonical Allele Identifier: CA1201830667
Gene: FCER1A HGNC NCBI

Linked Data

dbSNP Id: rs1652445402
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159302081_159302086del , CM000663.2:g.159302081_159302086del GRCh38
NC_000001.10:g.159271871_159271876del , CM000663.1:g.159271871_159271876del GRCh37
NC_000001.9:g.157538495_157538500del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368115.5:c.-59-225_-59-220del ENSP00000357097.1:n.-59-225_-59-220del
NM_002001.3:c.-59-225_-59-220del NP_001992.1:n.-59-225_-59-220del
NM_002001.4:c.-59-225_-59-220del NP_001992.1:n.-59-225_-59-220del
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