Canonical Allele Identifier: CA1488878445
Gene: FABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320521A= , CM000666.2:g.119320521A= GRCh38
NC_000004.11:g.120241676A= , CM000666.1:g.120241676A= GRCh37
NC_000004.10:g.120461124A= NCBI36
NG_011444.1:g.6641T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.240+149T= MANE Select ENSP00000274024.3:n.240+149T=
ENST00000274024.3:c.240+149T= ENSP00000274024.3:n.240+149T=
NM_000134.3:c.240+149T= NP_000125.2:n.240+149T=
NM_000134.4:c.240+149T= MANE Select NP_000125.2:n.240+149T=
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