Canonical Allele Identifier: CA786086739
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1472313535
gnomAD v4: 4-119320618-T-A
MyVariant Identifiers: chr4:g.120241773T>A (hg19) chr4:g.119320618T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320618T>A , CM000666.2:g.119320618T>A GRCh38
NC_000004.11:g.120241773T>A , CM000666.1:g.120241773T>A GRCh37
NC_000004.10:g.120461221T>A NCBI36
NG_011444.1:g.6544A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+52A>T MANE Select ENSP00000274024.3:n.240+52A>T
ENST00000274024.3:c.240+52A>T ENSP00000274024.3:n.240+52A>T
NM_000134.3:c.240+52A>T NP_000125.2:n.240+52A>T
NM_000134.4:c.240+52A>T MANE Select NP_000125.2:n.240+52A>T
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