Canonical Allele Identifier: CA10817846
Gene: ADCY10 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.167834585G>T
GRCh37 chr1:g.167803823G>T
gnomAD v2:
1:167803823 G / T
gnomAD v3:
1:167834585 G / T
gnomAD v4:
chr1-167834585-G-T
Joint Max Group AF 0.12139911 (EAS)
Genomes Max Group AF 0.1239437 (EAS)
Exomes Max Group AF 0.1111198 (EAS)
dbSNP:
3752608
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.167834585G>T , CM000663.2:g.167834585G>T GRCh38
NC_000001.10:g.167803823G>T , CM000663.1:g.167803823G>T GRCh37
NC_000001.9:g.166070447G>T NCBI36
NG_016139.1:g.84631C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367851.9:c.3310-508C>A MANE Select ENSP00000356825.4:n.3310-508C>A
ENST00000367848.1:c.3034-508C>A ENSP00000356822.1:n.3034-508C>A
ENST00000367851.8:c.3310-508C>A ENSP00000356825.4:n.3310-508C>A
ENST00000485964.5:c.809C>A
ENST00000545172.5:c.2851-508C>A ENSP00000441992.1:n.2851-508C>A
NM_001167749.2:c.2851-508C>A NP_001161221.1:n.2851-508C>A
NM_001297772.1:c.3034-508C>A NP_001284701.1:n.3034-508C>A
NM_018417.5:c.3310-508C>A NP_060887.2:n.3310-508C>A
XM_005245330.3:c.3310-508C>A XP_005245387.1:n.3310-508C>A
XM_006711449.2:c.3310-508C>A XP_006711512.1:n.3310-508C>A
XM_011509760.1:c.3310-508C>A XP_011508062.1:n.3310-508C>A
XM_011509761.1:c.3205-508C>A XP_011508063.1:n.3205-508C>A
XM_011509762.1:c.3166-508C>A XP_011508064.1:n.3166-508C>A
XM_011509763.1:c.3310-508C>A XP_011508065.1:n.3310-508C>A
XM_011509764.1:c.3061-508C>A XP_011508066.1:n.3061-508C>A
XM_011509765.1:c.3034-508C>A XP_011508067.1:n.3034-508C>A
XM_011509766.1:c.*101C>A XP_011508068.1:n.*101C>A
XR_921889.1:n.4919-508C>A
XM_005245330.5:c.3310-508C>A XP_005245387.1:n.3310-508C>A
XM_006711449.4:c.3310-508C>A XP_006711512.1:n.3310-508C>A
XM_011509760.3:c.3310-508C>A XP_011508062.1:n.3310-508C>A
XM_011509762.3:c.3166-508C>A XP_011508064.1:n.3166-508C>A
XM_011509763.3:c.3310-508C>A XP_011508065.1:n.3310-508C>A
XM_011509766.3:c.*101C>A XP_011508068.1:n.*101C>A
XM_017001778.2:c.3310-508C>A XP_016857267.1:n.3310-508C>A
XR_921889.3:n.5782-508C>A
NM_001167749.3:c.2851-508C>A NP_001161221.1:n.2851-508C>A
NM_001297772.2:c.3034-508C>A NP_001284701.1:n.3034-508C>A
NM_018417.6:c.3310-508C>A MANE Select NP_060887.2:n.3310-508C>A
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