Canonical Allele Identifier: CA1067271645
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1755649175
gnomAD v3: 4-119320544-T-C
gnomAD v4: 4-119320544-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320544T>C , CM000666.2:g.119320544T>C GRCh38
NC_000004.11:g.120241699T>C , CM000666.1:g.120241699T>C GRCh37
NC_000004.10:g.120461147T>C NCBI36
NG_011444.1:g.6618A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+126A>G MANE Select ENSP00000274024.3:n.240+126A>G
ENST00000274024.3:c.240+126A>G ENSP00000274024.3:n.240+126A>G
NM_000134.3:c.240+126A>G NP_000125.2:n.240+126A>G
NM_000134.4:c.240+126A>G MANE Select NP_000125.2:n.240+126A>G
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