Canonical Allele Identifier: CA358027589

Gene: FABP2

Linked Data

• dbSNP Id: rs1196338331
• gnomAD v2: 4-120241941-T-A
• gnomAD v4: 4-119320786-T-A
• MyVariant Identifiers: chr4:g.120241941T>A (hg19) ; chr4:g.119320786T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320786T>A , CM000666.2:g.119320786T>A	GRCh38
NC_000004.11:g.120241941T>A , CM000666.1:g.120241941T>A	GRCh37
NC_000004.10:g.120461389T>A	NCBI36
NG_011444.1:g.6376A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.124A>T MANE Select	ENSP00000274024.3:p.Thr42Ser
ENST00000274024.3:c.124A>T	ENSP00000274024.3:p.Thr42Ser
NM_000134.3:c.124A>T	NP_000125.2:p.Thr42Ser
NM_000134.4:c.124A>T MANE Select	NP_000125.2:p.Thr42Ser