Canonical Allele Identifier: CA1488878636
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755659496
gnomAD v4: 4-119320947-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320947T>A , CM000666.2:g.119320947T>A GRCh38
NC_000004.11:g.120242102T>A , CM000666.1:g.120242102T>A GRCh37
NC_000004.10:g.120461550T>A NCBI36
NG_011444.1:g.6215A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.68-105A>T MANE Select ENSP00000274024.3:n.68-105A>T
ENST00000274024.3:c.68-105A>T ENSP00000274024.3:n.68-105A>T
NM_000134.3:c.68-105A>T NP_000125.2:n.68-105A>T
NM_000134.4:c.68-105A>T MANE Select NP_000125.2:n.68-105A>T
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