Canonical Allele Identifier: CA358027976

Gene: FABP2

Linked Data

• dbSNP Id: rs1441305686
• gnomAD v3: 4-119320840-C-A
• gnomAD v4: 4-119320840-C-A
• MyVariant Identifiers: chr4:g.120241995C>A (hg19) ; chr4:g.119320840C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320840C>A , CM000666.2:g.119320840C>A	GRCh38
NC_000004.11:g.120241995C>A , CM000666.1:g.120241995C>A	GRCh37
NC_000004.10:g.120461443C>A	NCBI36
NG_011444.1:g.6322G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.70G>T MANE Select	ENSP00000274024.3:p.Val24Phe
ENST00000274024.3:c.70G>T	ENSP00000274024.3:p.Val24Phe
NM_000134.3:c.70G>T	NP_000125.2:p.Val24Phe
NM_000134.4:c.70G>T MANE Select	NP_000125.2:p.Val24Phe