Canonical Allele Identifier: CA1794673065
Gene: HNF4G HGNC NCBI

Linked Data

dbSNP Id: rs1807464706

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.75566445A>G , CM000670.2:g.75566445A>G GRCh38
NC_000008.10:g.76478680A>G , CM000670.1:g.76478680A>G GRCh37
NC_000008.9:g.76641235A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396423.4:c.*2349A>G MANE Select ENSP00000379701.3:n.*2349A>G
ENST00000674002.1:c.*2349A>G ENSP00000501146.1:n.*2349A>G
ENST00000396423.2:c.*2349A>G ENSP00000379701.2:n.*2349A>G
NM_004133.4:c.*2349A>G NP_004124.4:n.*2349A>G
XM_011517514.1:c.*2349A>G XP_011515816.1:n.*2349A>G
XM_011517515.1:c.*2349A>G XP_011515817.1:n.*2349A>G
XM_011517516.1:c.*2349A>G XP_011515818.1:n.*2349A>G
XM_011517517.1:c.*2349A>G XP_011515819.1:n.*2349A>G
XM_011517518.1:c.*2349A>G XP_011515820.1:n.*2349A>G
XM_011517519.1:c.*2349A>G XP_011515821.1:n.*2349A>G
XM_011517520.1:c.*2349A>G XP_011515822.1:n.*2349A>G
NM_001330561.1:c.*2349A>G NP_001317490.1:n.*2349A>G
NM_001330561.2:c.*2349A>G NP_001317490.1:n.*2349A>G
NM_004133.5:c.*2349A>G MANE Select NP_004124.5:n.*2349A>G