Canonical Allele Identifier: CA554157165

Gene: FABP2

Linked Data

• dbSNP Id: rs1215727230
• gnomAD v2: 4-120241819-T-A
• gnomAD v3: 4-119320664-T-A
• gnomAD v4: 4-119320664-T-A
• MyVariant Identifiers: chr4:g.120241819T>A (hg19) ; chr4:g.119320664T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320664T>A , CM000666.2:g.119320664T>A	GRCh38
NC_000004.11:g.120241819T>A , CM000666.1:g.120241819T>A	GRCh37
NC_000004.10:g.120461267T>A	NCBI36
NG_011444.1:g.6498A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000274024.4:c.240+6A>T MANE Select	ENSP00000274024.3:n.240+6A>T
ENST00000274024.3:c.240+6A>T	ENSP00000274024.3:n.240+6A>T
NM_000134.3:c.240+6A>T	NP_000125.2:n.240+6A>T
NM_000134.4:c.240+6A>T MANE Select	NP_000125.2:n.240+6A>T