Canonical Allele Identifier: CA890016197

Gene: FCER1A

Linked Data

• dbSNP Id: rs1398200428
• MyVariant Identifiers: chr1:g.159271708T>C (hg19) ; chr1:g.159301918T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159301918T>C , CM000663.2:g.159301918T>C	GRCh38
NC_000001.10:g.159271708T>C , CM000663.1:g.159271708T>C	GRCh37
NC_000001.9:g.157538332T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368115.5:c.-59-388T>C	ENSP00000357097.1:n.-59-388T>C
NM_002001.3:c.-59-388T>C	NP_001992.1:n.-59-388T>C
NM_002001.4:c.-59-388T>C	NP_001992.1:n.-59-388T>C