Canonical Allele Identifier: CA2616109661
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822582-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822582T>A , CM000673.2:g.116822582T>A GRCh38
NC_000011.9:g.116693298T>A , CM000673.1:g.116693298T>A GRCh37
NC_000011.8:g.116198508T>A NCBI36
NG_012044.1:g.5714A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.176+77A>T MANE Select ENSP00000350425.3:n.176+77A>T
ENST00000357780.4:c.176+77A>T ENSP00000350425.3:n.176+77A>T
NM_000482.3:c.176+77A>T NP_000473.2:n.176+77A>T
NM_000482.4:c.176+77A>T MANE Select NP_000473.2:n.176+77A>T
Search 100 bp 5'
Search 100 bp 3'