Canonical Allele Identifier: CA2648765017
Gene: FCER1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219149T>A , CM000663.2:g.161219149T>A GRCh38
NC_000001.10:g.161188939T>A , CM000663.1:g.161188939T>A GRCh37
NC_000001.9:g.159455563T>A NCBI36
NG_029043.1:g.8853T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*206T>A MANE Select ENSP00000289902.1:n.*206T>A
ENST00000289902.1:c.*206T>A ENSP00000289902.1:n.*206T>A
ENST00000367992.7:c.198+426T>A ENSP00000356971.3:n.198+426T>A
ENST00000490414.1:n.463T>A
NM_004106.1:c.*206T>A NP_004097.1:n.*206T>A
NM_004106.2:c.*206T>A MANE Select NP_004097.1:n.*206T>A