Canonical Allele Identifier: CA601825992
Gene: APOC3 HGNC NCBI

Linked Data

dbSNP Id: rs1313131097
gnomAD v2: 11-116703476-T-C
gnomAD v4: 11-116832760-T-C
MyVariant Identifiers: chr11:g.116703476T>C (hg19) chr11:g.116832760T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832760T>C , CM000673.2:g.116832760T>C GRCh38
NC_000011.9:g.116703476T>C , CM000673.1:g.116703476T>C GRCh37
NC_000011.8:g.116208686T>C NCBI36
NG_008949.1:g.7853T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.180-4T>C MANE Select ENSP00000227667.2:n.180-4T>C
ENST00000227667.7:c.180-4T>C ENSP00000227667.2:n.180-4T>C
ENST00000375345.3:c.234-4T>C ENSP00000364494.1:n.234-4T>C
ENST00000630701.1:c.234-4T>C ENSP00000486182.1:n.234-4T>C
NM_000040.1:c.180-4T>C NP_000031.1:n.180-4T>C
NM_000040.2:c.180-4T>C NP_000031.1:n.180-4T>C
NM_000040.3:c.180-4T>C MANE Select NP_000031.1:n.180-4T>C
Search 100 bp 5'
Search 100 bp 3'