Canonical Allele Identifier: CA397005622
Gene: FOXF1 HGNC NCBI

Linked Data

gnomAD v4: 16-86510804-C-G
MyVariant Identifiers: chr16:g.86544410C>G (hg19) chr16:g.86510804C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510804C>G , CM000678.2:g.86510804C>G GRCh38
NC_000016.9:g.86544410C>G , CM000678.1:g.86544410C>G GRCh37
NC_000016.8:g.85101911C>G NCBI36
NG_016273.1:g.5278C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.235C>G MANE Select ENSP00000262426.4:p.Gln79Glu
ENST00000262426.5:c.235C>G ENSP00000262426.4:p.Gln79Glu
NM_001451.2:c.235C>G NP_001442.2:p.Gln79Glu
NM_001451.3:c.235C>G MANE Select NP_001442.2:p.Gln79Glu
Search 100 bp 5'
Search 100 bp 3'