Canonical Allele Identifier: CA358026863
Gene: FABP2 HGNC NCBI

Linked Data

gnomAD v4: 4-119320697-G-T
MyVariant Identifiers: chr4:g.120241852G>T (hg19) chr4:g.119320697G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.119320697G>T , CM000666.2:g.119320697G>T GRCh38
NC_000004.11:g.120241852G>T , CM000666.1:g.120241852G>T GRCh37
NC_000004.10:g.120461300G>T NCBI36
NG_011444.1:g.6465C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274024.4:c.213C>A MANE Select ENSP00000274024.3:p.Tyr71Ter
ENST00000274024.3:c.213C>A ENSP00000274024.3:p.Tyr71Ter
NM_000134.3:c.213C>A NP_000125.2:p.Tyr71Ter
NM_000134.4:c.213C>A MANE Select NP_000125.2:p.Tyr71Ter
Search 100 bp 5'
Search 100 bp 3'