Canonical Allele Identifier: CA4711518
Gene: ADGRA2 HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.37829231A>G
GRCh37 chr8:g.37686749A>G
gnomAD v2:
8:37686749 A / G
gnomAD v3:
8:37829231 A / G
gnomAD v4:
chr8-37829231-A-G
Joint Max Group AF 0.94203486 (AFR)
Genomes Max Group AF 0.93818165 (AFR)
Exomes Max Group AF 0.94141401 (AFR)
dbSNP:
6468442
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.37829231A>G , CM000670.2:g.37829231A>G GRCh38
NC_000008.10:g.37686749A>G , CM000670.1:g.37686749A>G GRCh37
NC_000008.9:g.37805907A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412232.3:c.411-30A>G MANE Select ENSP00000406367.2:n.411-30A>G
ENST00000315215.11:c.411-30A>G ENSP00000323508.7:n.411-30A>G
ENST00000412232.2:c.411-30A>G ENSP00000406367.2:n.411-30A>G
ENST00000428068.5:c.285-30A>G ENSP00000400860.1:n.285-30A>G
NM_032777.9:c.411-30A>G NP_116166.9:n.411-30A>G
XM_005273471.3:c.411-30A>G XP_005273528.1:n.411-30A>G
XM_011544481.1:c.411-30A>G XP_011542783.1:n.411-30A>G
XM_011544482.1:c.339-30A>G XP_011542784.1:n.339-30A>G
XM_011544483.1:c.411-30A>G XP_011542785.1:n.411-30A>G
XM_011544481.2:c.411-30A>G XP_011542783.1:n.411-30A>G
XM_011544482.2:c.339-30A>G XP_011542784.1:n.339-30A>G
XM_011544483.2:c.411-30A>G XP_011542785.1:n.411-30A>G
NM_032777.10:c.411-30A>G MANE Select NP_116166.9:n.411-30A>G
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