Canonical Allele Identifier: CA358026724
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1480238944
gnomAD v2: 4-120241836-T-C
gnomAD v4: 4-119320681-T-C
MyVariant Identifiers: chr4:g.120241836T>C (hg19) chr4:g.119320681T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320681T>C , CM000666.2:g.119320681T>C GRCh38
NC_000004.11:g.120241836T>C , CM000666.1:g.120241836T>C GRCh37
NC_000004.10:g.120461284T>C NCBI36
NG_011444.1:g.6481A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.229A>G MANE Select ENSP00000274024.3:p.Thr77Ala
ENST00000274024.3:c.229A>G ENSP00000274024.3:p.Thr77Ala
NM_000134.3:c.229A>G NP_000125.2:p.Thr77Ala
NM_000134.4:c.229A>G MANE Select NP_000125.2:p.Thr77Ala
Search 100 bp 5'
Search 100 bp 3'