Canonical Allele Identifier: CA1067271677
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755649850
gnomAD v3: 4-119320572-T-G
gnomAD v4: 4-119320572-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320572T>G , CM000666.2:g.119320572T>G GRCh38
NC_000004.11:g.120241727T>G , CM000666.1:g.120241727T>G GRCh37
NC_000004.10:g.120461175T>G NCBI36
NG_011444.1:g.6590A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+98A>C MANE Select ENSP00000274024.3:n.240+98A>C
ENST00000274024.3:c.240+98A>C ENSP00000274024.3:n.240+98A>C
NM_000134.3:c.240+98A>C NP_000125.2:n.240+98A>C
NM_000134.4:c.240+98A>C MANE Select NP_000125.2:n.240+98A>C
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