Canonical Allele Identifier: CA3059775
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs367603528
ExAC: 4:120241839 C / T
gnomAD v2: 4-120241839-C-T
gnomAD v3: 4-119320684-C-T
gnomAD v4: 4-119320684-C-T
COSMIC: COSM3599554
MyVariant Identifiers: chr4:g.120241839C>T (hg19) chr4:g.119320684C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320684C>T , CM000666.2:g.119320684C>T GRCh38
NC_000004.11:g.120241839C>T , CM000666.1:g.120241839C>T GRCh37
NC_000004.10:g.120461287C>T NCBI36
NG_011444.1:g.6478G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.226G>A MANE Select ENSP00000274024.3:p.Gly76Arg
ENST00000274024.3:c.226G>A ENSP00000274024.3:p.Gly76Arg
NM_000134.3:c.226G>A NP_000125.2:p.Gly76Arg
NM_000134.4:c.226G>A MANE Select NP_000125.2:p.Gly76Arg
Search 100 bp 5'
Search 100 bp 3'