Canonical Allele Identifier: CA2671754
Gene: SUCNR1 HGNC NCBI
AADACL2-AS1 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.151881290C>G
GRCh37 chr3:g.151599078C>G
Revel Score:
ENST00000362032 (MANE Select) 0.432
gnomAD v2:
3:151599078 C / G
gnomAD v4:
chr3-151881290-C-G
Joint Max Group AF 0.00000553 (AMR)
Exomes Max Group AF 0.00000741 (AMR)
ClinVar RCV:
RCV004179760
ClinVar Variation:
2335475
dbSNP:
201481949
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.151881290C>G , CM000665.2:g.151881290C>G GRCh38
NC_000003.11:g.151599078C>G , CM000665.1:g.151599078C>G GRCh37
NC_000003.10:g.153081768C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000362032.6:c.747C>G (SUCNR1) MANE Select ENSP00000355156.4:p.His249Gln
NM_033050.4:c.747C>G (SUCNR1) NP_149039.2:p.His249Gln
NR_110202.1:n.319+46567G>C (AADACL2-AS1)
NR_110203.1:n.319+46567G>C (AADACL2-AS1)
NM_033050.5:c.747C>G (SUCNR1) NP_149039.2:p.His249Gln
NM_033050.6:c.747C>G (SUCNR1) MANE Select NP_149039.2:p.His249Gln
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