Canonical Allele Identifier: CA104693305

Gene: FABP2

Linked Data

• dbSNP Id: rs1044423839
• gnomAD v3: 4-119320443-T-C
• gnomAD v4: 4-119320443-T-C
• MyVariant Identifiers: chr4:g.120241598T>C (hg19) ; chr4:g.119320443T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320443T>C , CM000666.2:g.119320443T>C	GRCh38
NC_000004.11:g.120241598T>C , CM000666.1:g.120241598T>C	GRCh37
NC_000004.10:g.120461046T>C	NCBI36
NG_011444.1:g.6719A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.240+227A>G MANE Select	ENSP00000274024.3:n.240+227A>G
ENST00000274024.3:c.240+227A>G	ENSP00000274024.3:n.240+227A>G
NM_000134.3:c.240+227A>G	NP_000125.2:n.240+227A>G
NM_000134.4:c.240+227A>G MANE Select	NP_000125.2:n.240+227A>G