Canonical Allele Identifier: CA382705142
Gene: APOA4 HGNC NCBI

Linked Data

dbSNP Id: rs1941341268
MyVariant Identifiers: chr11:g.116693474T>C (hg19) chr11:g.116822758T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116822758T>C , CM000673.2:g.116822758T>C GRCh38
NC_000011.9:g.116693474T>C , CM000673.1:g.116693474T>C GRCh37
NC_000011.8:g.116198684T>C NCBI36
NG_012044.1:g.5538A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000357780.5:c.77A>G MANE Select ENSP00000350425.3:p.Gln26Arg
ENST00000357780.4:c.77A>G ENSP00000350425.3:p.Gln26Arg
NM_000482.3:c.77A>G NP_000473.2:p.Gln26Arg
NM_000482.4:c.77A>G MANE Select NP_000473.2:p.Gln26Arg
Search 100 bp 5'
Search 100 bp 3'