Canonical Allele Identifier: CA179861831

Gene: HNF4G

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.75505702A>G , CM000670.2:g.75505702A>G	GRCh38
NC_000008.10:g.76417937A>G , CM000670.1:g.76417937A>G	GRCh37
NC_000008.9:g.76580492A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354370.5:c.-24+15494A>G	ENSP00000346339.1:n.-24+15494A>G
ENST00000396419.5:n.143+15494A>G
ENST00000494318.5:n.295+10206A>G
XM_011517514.1:c.-24+10206A>G	XP_011515816.1:n.-24+10206A>G
XM_011517515.1:c.-24+10206A>G	XP_011515817.1:n.-24+10206A>G
XM_011517516.1:c.-24+15494A>G	XP_011515818.1:n.-24+15494A>G
XM_011517517.1:c.-24+10206A>G	XP_011515819.1:n.-24+10206A>G
XM_011517518.1:c.-24+10206A>G	XP_011515820.1:n.-24+10206A>G
XM_011517519.1:c.-24+10206A>G	XP_011515821.1:n.-24+10206A>G
XM_011517520.1:c.-24+15494A>G	XP_011515822.1:n.-24+15494A>G
NM_001330561.1:c.-24+15494A>G	NP_001317490.1:n.-24+15494A>G
XM_017013373.1:c.-24+15494A>G	XP_016868862.1:n.-24+15494A>G
XM_017013374.1:c.-24+15494A>G	XP_016868863.1:n.-24+15494A>G
XM_017013375.1:c.-24+15494A>G	XP_016868864.1:n.-24+15494A>G
XM_017013376.2:c.-24+15494A>G	XP_016868865.1:n.-24+15494A>G
NM_001330561.2:c.-24+15494A>G	NP_001317490.1:n.-24+15494A>G