Canonical Allele Identifier: CA2616109694
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs2134219155
gnomAD v4: 11-116822826-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822826T>C , CM000673.2:g.116822826T>C GRCh38
NC_000011.9:g.116693542T>C , CM000673.1:g.116693542T>C GRCh37
NC_000011.8:g.116198752T>C NCBI36
NG_012044.1:g.5470A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.50-41A>G MANE Select ENSP00000350425.3:n.50-41A>G
ENST00000357780.4:c.50-41A>G ENSP00000350425.3:n.50-41A>G
NM_000482.3:c.50-41A>G NP_000473.2:n.50-41A>G
NM_000482.4:c.50-41A>G MANE Select NP_000473.2:n.50-41A>G
Search 100 bp 5'
Search 100 bp 3'