Canonical Allele Identifier: CA466359992
Gene: FOXE1 HGNC NCBI

Linked Data

dbSNP Id: rs187644329
gnomAD v4: 9-97854001-C-G
MyVariant Identifiers: chr9:g.100616283C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97854001C>G , CM000671.2:g.97854001C>G GRCh38
NC_000009.11:g.100616283C>G , CM000671.1:g.100616283C>G GRCh37
NC_000009.10:g.99656104C>G NCBI36
NG_011979.1:g.5747C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375123.5:c.87C>G MANE Select ENSP00000364265.3:p.Ala29=
ENST00000375123.4:c.87C>G ENSP00000364265.3:p.Ala29=
NM_004473.3:c.87C>G NP_004464.2:p.Ala29=
NM_004473.4:c.87C>G MANE Select NP_004464.2:p.Ala29=
Search 100 bp 5'
Search 100 bp 3'