Canonical Allele Identifier: CA358026844
Gene: FABP2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.120241850T>G (hg19) chr4:g.119320695T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320695T>G , CM000666.2:g.119320695T>G GRCh38
NC_000004.11:g.120241850T>G , CM000666.1:g.120241850T>G GRCh37
NC_000004.10:g.120461298T>G NCBI36
NG_011444.1:g.6467A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.215A>C MANE Select ENSP00000274024.3:p.Asn72Thr
ENST00000274024.3:c.215A>C ENSP00000274024.3:p.Asn72Thr
NM_000134.3:c.215A>C NP_000125.2:p.Asn72Thr
NM_000134.4:c.215A>C MANE Select NP_000125.2:p.Asn72Thr
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