Canonical Allele Identifier: CA3059791
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs756398299
ExAC: 4:120241934 T / A
gnomAD v2: 4-120241934-T-A
gnomAD v3: 4-119320779-T-A
gnomAD v4: 4-119320779-T-A
MyVariant Identifiers: chr4:g.120241934T>A (hg19) chr4:g.119320779T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320779T>A , CM000666.2:g.119320779T>A GRCh38
NC_000004.11:g.120241934T>A , CM000666.1:g.120241934T>A GRCh37
NC_000004.10:g.120461382T>A NCBI36
NG_011444.1:g.6383A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.131A>T MANE Select ENSP00000274024.3:p.Glu44Val
ENST00000274024.3:c.131A>T ENSP00000274024.3:p.Glu44Val
NM_000134.3:c.131A>T NP_000125.2:p.Glu44Val
NM_000134.4:c.131A>T MANE Select NP_000125.2:p.Glu44Val
Search 100 bp 5'
Search 100 bp 3'