Canonical Allele Identifier: CA2671636

Gene: SUCNR1 AADACL2-AS1

Linked Data

• ClinVar Variation Id: 2600691
• ClinVar RCV Id: RCV004349636
• dbSNP Id: rs540877223
• ExAC: 3:151598418 T / G
• gnomAD v2: 3-151598418-T-G
• gnomAD v3: 3-151880630-T-G
• gnomAD v4: 3-151880630-T-G
• MyVariant Identifiers: chr3:g.151598418T>G (hg19) ; chr3:g.151880630T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.151880630T>G , CM000665.2:g.151880630T>G	GRCh38
NC_000003.11:g.151598418T>G , CM000665.1:g.151598418T>G	GRCh37
NC_000003.10:g.153081108T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362032.6:c.87T>G (SUCNR1) MANE Select	ENSP00000355156.4:p.Phe29Leu
NM_033050.4:c.87T>G (SUCNR1)	NP_149039.2:p.Phe29Leu
NR_110202.1:n.319+47227A>C (AADACL2-AS1)
NR_110203.1:n.319+47227A>C (AADACL2-AS1)
NM_033050.5:c.87T>G (SUCNR1)	NP_149039.2:p.Phe29Leu
NM_033050.6:c.87T>G (SUCNR1) MANE Select	NP_149039.2:p.Phe29Leu