Canonical Allele Identifier: CA397005582
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544401C>T (hg19) chr16:g.86510795C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510795C>T , CM000678.2:g.86510795C>T GRCh38
NC_000016.9:g.86544401C>T , CM000678.1:g.86544401C>T GRCh37
NC_000016.8:g.85101902C>T NCBI36
NG_016273.1:g.5269C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.226C>T MANE Select ENSP00000262426.4:p.Gln76Ter
ENST00000262426.5:c.226C>T ENSP00000262426.4:p.Gln76Ter
NM_001451.2:c.226C>T NP_001442.2:p.Gln76Ter
NM_001451.3:c.226C>T MANE Select NP_001442.2:p.Gln76Ter
Search 100 bp 5'
Search 100 bp 3'