Canonical Allele Identifier: CA466360015
Gene: FOXE1 HGNC NCBI

Linked Data

gnomAD v4: 9-97854013-G-T
MyVariant Identifiers: chr9:g.100616295G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97854013G>T , CM000671.2:g.97854013G>T GRCh38
NC_000009.11:g.100616295G>T , CM000671.1:g.100616295G>T GRCh37
NC_000009.10:g.99656116G>T NCBI36
NG_011979.1:g.5759G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.99G>T MANE Select ENSP00000364265.3:p.Gly33=
ENST00000375123.4:c.99G>T ENSP00000364265.3:p.Gly33=
NM_004473.3:c.99G>T NP_004464.2:p.Gly33=
NM_004473.4:c.99G>T MANE Select NP_004464.2:p.Gly33=
Search 100 bp 5'
Search 100 bp 3'