Canonical Allele Identifier: CA2648764917
Gene: FCER1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219078A>G , CM000663.2:g.161219078A>G GRCh38
NC_000001.10:g.161188868A>G , CM000663.1:g.161188868A>G GRCh37
NC_000001.9:g.159455492A>G NCBI36
NG_029043.1:g.8782A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*135A>G MANE Select ENSP00000289902.1:n.*135A>G
ENST00000289902.1:c.*135A>G ENSP00000289902.1:n.*135A>G
ENST00000367992.7:c.198+355A>G ENSP00000356971.3:n.198+355A>G
ENST00000490414.1:n.392A>G
NM_004106.1:c.*135A>G NP_004097.1:n.*135A>G
NM_004106.2:c.*135A>G MANE Select NP_004097.1:n.*135A>G