Canonical Allele Identifier: CA497013736
Gene: FOXF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.86544367A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.86510761A>T , CM000678.2:g.86510761A>T GRCh38
NC_000016.9:g.86544367A>T , CM000678.1:g.86544367A>T GRCh37
NC_000016.8:g.85101868A>T NCBI36
NG_016273.1:g.5235A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262426.6:c.192A>T MANE Select ENSP00000262426.4:p.Ser64=
ENST00000262426.5:c.192A>T ENSP00000262426.4:p.Ser64=
NM_001451.2:c.192A>T NP_001442.2:p.Ser64=
NM_001451.3:c.192A>T MANE Select NP_001442.2:p.Ser64=