Canonical Allele Identifier: CA2648764891
Gene: FCER1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219047C>T , CM000663.2:g.161219047C>T GRCh38
NC_000001.10:g.161188837C>T , CM000663.1:g.161188837C>T GRCh37
NC_000001.9:g.159455461C>T NCBI36
NG_029043.1:g.8751C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*104C>T MANE Select ENSP00000289902.1:n.*104C>T
ENST00000289902.1:c.*104C>T ENSP00000289902.1:n.*104C>T
ENST00000367992.7:c.198+324C>T ENSP00000356971.3:n.198+324C>T
ENST00000490414.1:n.361C>T
NM_004106.1:c.*104C>T NP_004097.1:n.*104C>T
NM_004106.2:c.*104C>T MANE Select NP_004097.1:n.*104C>T