Canonical Allele Identifier: CA3059777
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs546773434
ExAC: 4:120241842 C / T
gnomAD v2: 4-120241842-C-T
gnomAD v3: 4-119320687-C-T
gnomAD v4: 4-119320687-C-T
MyVariant Identifiers: chr4:g.120241842C>T (hg19) chr4:g.119320687C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320687C>T , CM000666.2:g.119320687C>T GRCh38
NC_000004.11:g.120241842C>T , CM000666.1:g.120241842C>T GRCh37
NC_000004.10:g.120461290C>T NCBI36
NG_011444.1:g.6475G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.223G>A MANE Select ENSP00000274024.3:p.Asp75Asn
ENST00000274024.3:c.223G>A ENSP00000274024.3:p.Asp75Asn
NM_000134.3:c.223G>A NP_000125.2:p.Asp75Asn
NM_000134.4:c.223G>A MANE Select NP_000125.2:p.Asp75Asn
Search 100 bp 5'
Search 100 bp 3'