Canonical Allele Identifier: CA440891030
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241930T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320775T>C , CM000666.2:g.119320775T>C GRCh38
NC_000004.11:g.120241930T>C , CM000666.1:g.120241930T>C GRCh37
NC_000004.10:g.120461378T>C NCBI36
NG_011444.1:g.6387A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.135A>G MANE Select ENSP00000274024.3:p.Gly45=
ENST00000274024.3:c.135A>G ENSP00000274024.3:p.Gly45=
NM_000134.3:c.135A>G NP_000125.2:p.Gly45=
NM_000134.4:c.135A>G MANE Select NP_000125.2:p.Gly45=
Search 100 bp 5'
Search 100 bp 3'