Canonical Allele Identifier: CA1797411942
Gene: FABP4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478440T= , CM000670.2:g.81478440T= GRCh38
NC_000008.10:g.82390675T= , CM000670.1:g.82390675T= GRCh37
NC_000008.9:g.82553230T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*425A= MANE Select ENSP00000256104.4:n.*425A=
ENST00000256104.4:c.*425A= ENSP00000256104.4:n.*425A=
XR_001745980.1:n.514+16466T=
NM_001442.3:c.*425A= MANE Select NP_001433.1:n.*425A=
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