Canonical Allele Identifier: CA1127209713
Gene: FOXE1 HGNC NCBI

Linked Data

dbSNP Id: rs1830623679
gnomAD v3: 9-97853891-C-T
gnomAD v4: 9-97853891-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97853891C>T , CM000671.2:g.97853891C>T GRCh38
NC_000009.11:g.100616173C>T , CM000671.1:g.100616173C>T GRCh37
NC_000009.10:g.99655994C>T NCBI36
NG_011979.1:g.5637C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375123.5:c.-24C>T MANE Select ENSP00000364265.3:n.-24C>T
ENST00000375123.4:c.-24C>T ENSP00000364265.3:n.-24C>T
NM_004473.3:c.-24C>T NP_004464.2:n.-24C>T
NM_004473.4:c.-24C>T MANE Select NP_004464.2:n.-24C>T
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