Canonical Allele Identifier: CA890016224

Gene: FCER1A

Linked Data

• dbSNP Id: rs1371166168
• MyVariant Identifiers: chr1:g.159271759C>T (hg19) ; chr1:g.159301969C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159301969C>T , CM000663.2:g.159301969C>T	GRCh38
NC_000001.10:g.159271759C>T , CM000663.1:g.159271759C>T	GRCh37
NC_000001.9:g.157538383C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000368115.5:c.-59-337C>T	ENSP00000357097.1:n.-59-337C>T
NM_002001.3:c.-59-337C>T	NP_001992.1:n.-59-337C>T
NM_002001.4:c.-59-337C>T	NP_001992.1:n.-59-337C>T