Canonical Allele Identifier: CA786086726
Gene: FABP2 HGNC NCBI

Linked Data

dbSNP Id: rs1315330580
gnomAD v3: 4-119320560-G-A
gnomAD v4: 4-119320560-G-A
MyVariant Identifiers: chr4:g.120241715G>A (hg19) chr4:g.119320560G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320560G>A , CM000666.2:g.119320560G>A GRCh38
NC_000004.11:g.120241715G>A , CM000666.1:g.120241715G>A GRCh37
NC_000004.10:g.120461163G>A NCBI36
NG_011444.1:g.6602C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274024.4:c.240+110C>T MANE Select ENSP00000274024.3:n.240+110C>T
ENST00000274024.3:c.240+110C>T ENSP00000274024.3:n.240+110C>T
NM_000134.3:c.240+110C>T NP_000125.2:n.240+110C>T
NM_000134.4:c.240+110C>T MANE Select NP_000125.2:n.240+110C>T
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