Canonical Allele Identifier: CA362558696

Gene: FOXC1

Linked Data

• MyVariant Identifiers: chr6:g.1611063A>C (hg19) ; chr6:g.1610828A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1610828A>C , CM000668.2:g.1610828A>C	GRCh38
NC_000006.11:g.1611063A>C , CM000668.1:g.1611063A>C	GRCh37
NC_000006.10:g.1556062A>C	NCBI36
NG_009368.1:g.5383A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645831.2:c.383A>C MANE Select	ENSP00000493906.1:p.His128Pro
ENST00000380874.3:c.383A>C	ENSP00000370256.2:p.His128Pro
NM_001453.2:c.383A>C	NP_001444.2:p.His128Pro
NM_001453.3:c.383A>C MANE Select	NP_001444.2:p.His128Pro