Canonical Allele Identifier: CA3059794
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs747585151
ExAC: 4:120241957 ATTGTCATG / A
gnomAD v2: 4-120241957-ATTGTCATG-A
MyVariant Identifiers: chr4:g.120241958_120241965del (hg19) chr4:g.119320803_119320810del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320803_119320810del , CM000666.2:g.119320803_119320810del GRCh38
NC_000004.11:g.120241958_120241965del , CM000666.1:g.120241958_120241965del GRCh37
NC_000004.10:g.120461406_120461413del NCBI36
NG_011444.1:g.6352_6359del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.100_107del MANE Select ENSP00000274024.3:p.His34PhefsTer11
ENST00000274024.3:c.100_107del ENSP00000274024.3:p.His34PhefsTer11
NM_000134.3:c.100_107del NP_000125.2:p.His34PhefsTer11
NM_000134.4:c.100_107del MANE Select NP_000125.2:p.His34PhefsTer11
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