Canonical Allele Identifier: CA2648765057
Gene: FCER1G HGNC NCBI

Linked Data

gnomAD v4: 1-161219162-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161219162T>A , CM000663.2:g.161219162T>A GRCh38
NC_000001.10:g.161188952T>A , CM000663.1:g.161188952T>A GRCh37
NC_000001.9:g.159455576T>A NCBI36
NG_029043.1:g.8866T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000289902.2:c.*219T>A MANE Select ENSP00000289902.1:n.*219T>A
ENST00000289902.1:c.*219T>A ENSP00000289902.1:n.*219T>A
ENST00000367992.7:c.198+439T>A ENSP00000356971.3:n.198+439T>A
ENST00000490414.1:n.476T>A
NM_004106.1:c.*219T>A NP_004097.1:n.*219T>A
NM_004106.2:c.*219T>A MANE Select NP_004097.1:n.*219T>A
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