Canonical Allele Identifier: CA786086731
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1297027450
gnomAD v4: 4-119320579-A-G
MyVariant Identifiers: chr4:g.120241734A>G (hg19) chr4:g.119320579A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320579A>G , CM000666.2:g.119320579A>G GRCh38
NC_000004.11:g.120241734A>G , CM000666.1:g.120241734A>G GRCh37
NC_000004.10:g.120461182A>G NCBI36
NG_011444.1:g.6583T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+91T>C MANE Select ENSP00000274024.3:n.240+91T>C
ENST00000274024.3:c.240+91T>C ENSP00000274024.3:n.240+91T>C
NM_000134.3:c.240+91T>C NP_000125.2:n.240+91T>C
NM_000134.4:c.240+91T>C MANE Select NP_000125.2:n.240+91T>C
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