Canonical Allele Identifier: CA597562672
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs1401817703
gnomAD v2: 11-10390627-A-G
gnomAD v3: 11-10369080-A-G
gnomAD v4: 11-10369080-A-G
MyVariant Identifiers: chr11:g.10390627A>G (hg19) chr11:g.10369080A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10369080A>G , CM000673.2:g.10369080A>G GRCh38
NC_000011.9:g.10390627A>G , CM000673.1:g.10390627A>G GRCh37
NC_000011.8:g.10347203A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295663.9:n.51-23202A>G
ENST00000527261.5:n.501+38371A>G
ENST00000532250.5:c.-6+38371A>G ENSP00000432707.1:n.-6+38371A>G
ENST00000532966.1:n.119+11689A>G
NR_103765.1:n.501+38371A>G
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