Canonical Allele Identifier: CA104693282

Gene: FABP2

Linked Data

• dbSNP Id: rs998659241
• gnomAD v2: 4-120241562-G-A
• gnomAD v3: 4-119320407-G-A
• gnomAD v4: 4-119320407-G-A
• MyVariant Identifiers: chr4:g.120241562G>A (hg19) ; chr4:g.119320407G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320407G>A , CM000666.2:g.119320407G>A	GRCh38
NC_000004.11:g.120241562G>A , CM000666.1:g.120241562G>A	GRCh37
NC_000004.10:g.120461010G>A	NCBI36
NG_011444.1:g.6755C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.240+263C>T MANE Select	ENSP00000274024.3:n.240+263C>T
ENST00000274024.3:c.240+263C>T	ENSP00000274024.3:n.240+263C>T
NM_000134.3:c.240+263C>T	NP_000125.2:n.240+263C>T
NM_000134.4:c.240+263C>T MANE Select	NP_000125.2:n.240+263C>T