Canonical Allele Identifier: CA652474102
Gene: FABP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478730T>C , CM000670.2:g.81478730T>C GRCh38
NC_000008.10:g.82390965T>C , CM000670.1:g.82390965T>C GRCh37
NC_000008.9:g.82553520T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*135A>G MANE Select ENSP00000256104.4:n.*135A>G
ENST00000256104.4:c.*135A>G ENSP00000256104.4:n.*135A>G
ENST00000518669.5:n.469A>G
ENST00000521734.1:n.743A>G
ENST00000522659.1:c.*410A>G ENSP00000428385.1:n.*410A>G
NM_001442.2:c.*135A>G NP_001433.1:n.*135A>G
XR_001745980.1:n.514+16756T>C
NM_001442.3:c.*135A>G MANE Select NP_001433.1:n.*135A>G