Canonical Allele Identifier: CA2687741731
Gene: FABP4 HGNC NCBI

Linked Data

gnomAD v4: 8-81478766-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478766G>T , CM000670.2:g.81478766G>T GRCh38
NC_000008.10:g.82391001G>T , CM000670.1:g.82391001G>T GRCh37
NC_000008.9:g.82553556G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*99C>A MANE Select ENSP00000256104.4:n.*99C>A
ENST00000256104.4:c.*99C>A ENSP00000256104.4:n.*99C>A
ENST00000518669.5:n.433C>A
ENST00000521734.1:n.707C>A
ENST00000522659.1:c.*374C>A ENSP00000428385.1:n.*374C>A
NM_001442.2:c.*99C>A NP_001433.1:n.*99C>A
XR_001745980.1:n.514+16792G>T
NM_001442.3:c.*99C>A MANE Select NP_001433.1:n.*99C>A
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