Canonical Allele Identifier: CA2648764961

Gene: FCER1G

Linked Data

• gnomAD v4: 1-161219112-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161219112A>T , CM000663.2:g.161219112A>T	GRCh38
NC_000001.10:g.161188902A>T , CM000663.1:g.161188902A>T	GRCh37
NC_000001.9:g.159455526A>T	NCBI36
NG_029043.1:g.8816A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289902.2:c.*169A>T MANE Select	ENSP00000289902.1:n.*169A>T
ENST00000289902.1:c.*169A>T	ENSP00000289902.1:n.*169A>T
ENST00000367992.7:c.198+389A>T	ENSP00000356971.3:n.198+389A>T
ENST00000490414.1:n.426A>T
NM_004106.1:c.*169A>T	NP_004097.1:n.*169A>T
NM_004106.2:c.*169A>T MANE Select	NP_004097.1:n.*169A>T