Canonical Allele Identifier: CA2616109656
Gene: APOA4 HGNC NCBI

Linked Data

gnomAD v4: 11-116822569-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822569G>C , CM000673.2:g.116822569G>C GRCh38
NC_000011.9:g.116693285G>C , CM000673.1:g.116693285G>C GRCh37
NC_000011.8:g.116198495G>C NCBI36
NG_012044.1:g.5727C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.176+90C>G MANE Select ENSP00000350425.3:n.176+90C>G
ENST00000357780.4:c.176+90C>G ENSP00000350425.3:n.176+90C>G
NM_000482.3:c.176+90C>G NP_000473.2:n.176+90C>G
NM_000482.4:c.176+90C>G MANE Select NP_000473.2:n.176+90C>G
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