Canonical Allele Identifier: CA1797412221
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1808010273
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478744C>G , CM000670.2:g.81478744C>G GRCh38
NC_000008.10:g.82390979C>G , CM000670.1:g.82390979C>G GRCh37
NC_000008.9:g.82553534C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*121G>C MANE Select ENSP00000256104.4:n.*121G>C
ENST00000256104.4:c.*121G>C ENSP00000256104.4:n.*121G>C
ENST00000518669.5:n.455G>C
ENST00000521734.1:n.729G>C
ENST00000522659.1:c.*396G>C ENSP00000428385.1:n.*396G>C
NM_001442.2:c.*121G>C NP_001433.1:n.*121G>C
XR_001745980.1:n.514+16770C>G
NM_001442.3:c.*121G>C MANE Select NP_001433.1:n.*121G>C
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