Canonical Allele Identifier: CA602136461

Gene: APOC3

Linked Data

• dbSNP Id: rs1484473447
• gnomAD v2: 11-116701363-T-C
• gnomAD v3: 11-116830647-T-C
• gnomAD v4: 11-116830647-T-C
• MyVariant Identifiers: chr11:g.116701363T>C (hg19) ; chr11:g.116830647T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830647T>C , CM000673.2:g.116830647T>C	GRCh38
NC_000011.9:g.116701363T>C , CM000673.1:g.116701363T>C	GRCh37
NC_000011.8:g.116206573T>C	NCBI36
NG_008949.1:g.5740T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.55+10T>C MANE Select	ENSP00000227667.2:n.55+10T>C
ENST00000227667.7:c.55+10T>C	ENSP00000227667.2:n.55+10T>C
ENST00000375345.3:c.109+10T>C	ENSP00000364494.1:n.109+10T>C
ENST00000433777.5:c.55+10T>C	ENSP00000410614.1:n.55+10T>C
ENST00000470144.1:n.87+10T>C
ENST00000630701.1:c.109+10T>C	ENSP00000486182.1:n.109+10T>C
NM_000040.1:c.55+10T>C	NP_000031.1:n.55+10T>C
NM_000040.2:c.55+10T>C	NP_000031.1:n.55+10T>C
NM_000040.3:c.55+10T>C MANE Select	NP_000031.1:n.55+10T>C