Canonical Allele Identifier: CA2648765053
Gene: FCER1G HGNC NCBI

Linked Data

gnomAD v4: 1-161219160-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219160T>C , CM000663.2:g.161219160T>C GRCh38
NC_000001.10:g.161188950T>C , CM000663.1:g.161188950T>C GRCh37
NC_000001.9:g.159455574T>C NCBI36
NG_029043.1:g.8864T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*217T>C MANE Select ENSP00000289902.1:n.*217T>C
ENST00000289902.1:c.*217T>C ENSP00000289902.1:n.*217T>C
ENST00000367992.7:c.198+437T>C ENSP00000356971.3:n.198+437T>C
ENST00000490414.1:n.474T>C
NM_004106.1:c.*217T>C NP_004097.1:n.*217T>C
NM_004106.2:c.*217T>C MANE Select NP_004097.1:n.*217T>C
Search 100 bp 5'
Search 100 bp 3'