Canonical Allele Identifier: CA382706625
Gene: APOA4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.116693502C>A (hg19) chr11:g.116822786C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822786C>A , CM000673.2:g.116822786C>A GRCh38
NC_000011.9:g.116693502C>A , CM000673.1:g.116693502C>A GRCh37
NC_000011.8:g.116198712C>A NCBI36
NG_012044.1:g.5510G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000357780.5:c.50-1G>T MANE Select ENSP00000350425.3:n.50-1G>T
ENST00000357780.4:c.50-1G>T ENSP00000350425.3:n.50-1G>T
NM_000482.3:c.50-1G>T NP_000473.2:n.50-1G>T
NM_000482.4:c.50-1G>T MANE Select NP_000473.2:n.50-1G>T
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