Canonical Allele Identifier: CA869017142
Gene: FOXE1 HGNC NCBI

Linked Data

dbSNP Id: rs1261466851
gnomAD v3: 9-97855110-A-G
gnomAD v4: 9-97855110-A-G
MyVariant Identifiers: chr9:g.100617392A>G (hg19) chr9:g.97855110A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97855110A>G , CM000671.2:g.97855110A>G GRCh38
NC_000009.11:g.100617392A>G , CM000671.1:g.100617392A>G GRCh37
NC_000009.10:g.99657213A>G NCBI36
NG_011979.1:g.6856A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.*74A>G MANE Select ENSP00000364265.3:n.*74A>G
ENST00000375123.4:c.*74A>G ENSP00000364265.3:n.*74A>G
NM_004473.3:c.*74A>G NP_004464.2:n.*74A>G
NM_004473.4:c.*74A>G MANE Select NP_004464.2:n.*74A>G
Search 100 bp 5'
Search 100 bp 3'