Canonical Allele Identifier: CA3059806
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs200065369
ExAC: 4:120242032 A / C
gnomAD v2: 4-120242032-A-C
gnomAD v3: 4-119320877-A-C
gnomAD v4: 4-119320877-A-C
MyVariant Identifiers: chr4:g.120242032A>C (hg19) chr4:g.119320877A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320877A>C , CM000666.2:g.119320877A>C GRCh38
NC_000004.11:g.120242032A>C , CM000666.1:g.120242032A>C GRCh37
NC_000004.10:g.120461480A>C NCBI36
NG_011444.1:g.6285T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.68-35T>G MANE Select ENSP00000274024.3:n.68-35T>G
ENST00000274024.3:c.68-35T>G ENSP00000274024.3:n.68-35T>G
NM_000134.3:c.68-35T>G NP_000125.2:n.68-35T>G
NM_000134.4:c.68-35T>G MANE Select NP_000125.2:n.68-35T>G
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