Canonical Allele Identifier: CA358027909
Gene: FABP2 HGNC NCBI

Linked Data

gnomAD v4: 4-119320831-C-G
MyVariant Identifiers: chr4:g.120241986C>G (hg19) chr4:g.119320831C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320831C>G , CM000666.2:g.119320831C>G GRCh38
NC_000004.11:g.120241986C>G , CM000666.1:g.120241986C>G GRCh37
NC_000004.10:g.120461434C>G NCBI36
NG_011444.1:g.6331G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.79G>C MANE Select ENSP00000274024.3:p.Val27Leu
ENST00000274024.3:c.79G>C ENSP00000274024.3:p.Val27Leu
NM_000134.3:c.79G>C NP_000125.2:p.Val27Leu
NM_000134.4:c.79G>C MANE Select NP_000125.2:p.Val27Leu
Search 100 bp 5'
Search 100 bp 3'