Canonical Allele Identifier: CA180381961
Gene: FABP4 HGNC NCBI

Linked Data

dbSNP Id: rs1024422510
gnomAD v2: 8-82390964-A-G
gnomAD v3: 8-81478729-A-G
gnomAD v4: 8-81478729-A-G
MyVariant Identifiers: chr8:g.82390964A>G (hg19) chr8:g.81478729A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.81478729A>G , CM000670.2:g.81478729A>G GRCh38
NC_000008.10:g.82390964A>G , CM000670.1:g.82390964A>G GRCh37
NC_000008.9:g.82553519A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256104.5:c.*136T>C MANE Select ENSP00000256104.4:n.*136T>C
ENST00000256104.4:c.*136T>C ENSP00000256104.4:n.*136T>C
ENST00000518669.5:n.470T>C
ENST00000521734.1:n.744T>C
ENST00000522659.1:c.*411T>C ENSP00000428385.1:n.*411T>C
NM_001442.2:c.*136T>C NP_001433.1:n.*136T>C
XR_001745980.1:n.514+16755A>G
NM_001442.3:c.*136T>C MANE Select NP_001433.1:n.*136T>C
Search 100 bp 5'
Search 100 bp 3'