Canonical Allele Identifier: CA180381953

Gene: FABP4

Linked Data

• dbSNP Id: rs150699129
• gnomAD v2: 8-82390954-A-G
• gnomAD v3: 8-81478719-A-G
• gnomAD v4: 8-81478719-A-G
• MyVariant Identifiers: chr8:g.82390954A>G (hg19) ; chr8:g.81478719A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.81478719A>G , CM000670.2:g.81478719A>G	GRCh38
NC_000008.10:g.82390954A>G , CM000670.1:g.82390954A>G	GRCh37
NC_000008.9:g.82553509A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256104.5:c.*146T>C MANE Select	ENSP00000256104.4:n.*146T>C
ENST00000256104.4:c.*146T>C	ENSP00000256104.4:n.*146T>C
ENST00000518669.5:n.480T>C
ENST00000521734.1:n.754T>C
ENST00000522659.1:c.*421T>C	ENSP00000428385.1:n.*421T>C
NM_001442.2:c.*146T>C	NP_001433.1:n.*146T>C
XR_001745980.1:n.514+16745A>G
NM_001442.3:c.*146T>C MANE Select	NP_001433.1:n.*146T>C