Canonical Allele Identifier: CA1797412228
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1808010457
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478756T>G , CM000670.2:g.81478756T>G GRCh38
NC_000008.10:g.82390991T>G , CM000670.1:g.82390991T>G GRCh37
NC_000008.9:g.82553546T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*109A>C MANE Select ENSP00000256104.4:n.*109A>C
ENST00000256104.4:c.*109A>C ENSP00000256104.4:n.*109A>C
ENST00000518669.5:n.443A>C
ENST00000521734.1:n.717A>C
ENST00000522659.1:c.*384A>C ENSP00000428385.1:n.*384A>C
NM_001442.2:c.*109A>C NP_001433.1:n.*109A>C
XR_001745980.1:n.514+16782T>G
NM_001442.3:c.*109A>C MANE Select NP_001433.1:n.*109A>C
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