Canonical Allele Identifier: CA890013241

Gene: FCER1A

Linked Data

• dbSNP Id: rs1320152010
• MyVariant Identifiers: chr1:g.159258491G>C (hg19) ; chr1:g.159288701G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159288701G>C , CM000663.2:g.159288701G>C	GRCh38
NC_000001.10:g.159258491G>C , CM000663.1:g.159258491G>C	GRCh37
NC_000001.9:g.157525115G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_002001.3:c.-97-1015G>C	NP_001992.1:n.-97-1015G>C
NM_002001.4:c.-97-1015G>C	NP_001992.1:n.-97-1015G>C