Canonical Allele Identifier: CA2648764894
Gene: FCER1G HGNC NCBI

Linked Data

gnomAD v4: 1-161219049-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219049C>A , CM000663.2:g.161219049C>A GRCh38
NC_000001.10:g.161188839C>A , CM000663.1:g.161188839C>A GRCh37
NC_000001.9:g.159455463C>A NCBI36
NG_029043.1:g.8753C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000289902.2:c.*106C>A MANE Select ENSP00000289902.1:n.*106C>A
ENST00000289902.1:c.*106C>A ENSP00000289902.1:n.*106C>A
ENST00000367992.7:c.198+326C>A ENSP00000356971.3:n.198+326C>A
ENST00000490414.1:n.363C>A
NM_004106.1:c.*106C>A NP_004097.1:n.*106C>A
NM_004106.2:c.*106C>A MANE Select NP_004097.1:n.*106C>A
Search 100 bp 5'
Search 100 bp 3'