Canonical Allele Identifier: CA12321068
Gene: DDAH2 HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.31730311T>G
GRCh37 chr6:g.31698088T>G
gnomAD v2:
6:31698088 T / G
gnomAD v3:
6:31730311 T / G
gnomAD v4:
chr6-31730311-T-G
Joint Max Group AF 0.69886505 (AFR)
Genomes Max Group AF 0.69883028 (AFR)
Exomes Max Group AF 0.64910792 (AFR)
dbSNP:
805304
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31730311T>G , CM000668.2:g.31730311T>G GRCh38
NC_000006.11:g.31698088T>G , CM000668.1:g.31698088T>G GRCh37
NC_000006.10:g.31806067T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000375792.7:c.-325A>C ENSP00000364949.3:n.-325A>C
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