Canonical Allele Identifier: CA104693313

Gene: FABP2

Linked Data

• dbSNP Id: rs939163240
• gnomAD v3: 4-119320476-C-T
• gnomAD v4: 4-119320476-C-T
• MyVariant Identifiers: chr4:g.120241631C>T (hg19) ; chr4:g.119320476C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.119320476C>T , CM000666.2:g.119320476C>T	GRCh38
NC_000004.11:g.120241631C>T , CM000666.1:g.120241631C>T	GRCh37
NC_000004.10:g.120461079C>T	NCBI36
NG_011444.1:g.6686G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274024.4:c.240+194G>A MANE Select	ENSP00000274024.3:n.240+194G>A
ENST00000274024.3:c.240+194G>A	ENSP00000274024.3:n.240+194G>A
NM_000134.3:c.240+194G>A	NP_000125.2:n.240+194G>A
NM_000134.4:c.240+194G>A MANE Select	NP_000125.2:n.240+194G>A