Canonical Allele Identifier: CA217639803
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs186882621
gnomAD v2: 11-10390592-C-A
gnomAD v3: 11-10369045-C-A
gnomAD v4: 11-10369045-C-A
MyVariant Identifiers: chr11:g.10390592C>A (hg19) chr11:g.10369045C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10369045C>A , CM000673.2:g.10369045C>A GRCh38
NC_000011.9:g.10390592C>A , CM000673.1:g.10390592C>A GRCh37
NC_000011.8:g.10347168C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295663.9:n.51-23237C>A
ENST00000527261.5:n.501+38336C>A
ENST00000532250.5:c.-6+38336C>A ENSP00000432707.1:n.-6+38336C>A
ENST00000532966.1:n.119+11654C>A
NR_103765.1:n.501+38336C>A
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