Canonical Allele Identifier: CA670944821
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs1188471982
gnomAD v3: 11-10329016-C-G
gnomAD v4: 11-10329016-C-G
MyVariant Identifiers: chr11:g.10350563C>G (hg19) chr11:g.10329016C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10329016C>G , CM000673.2:g.10329016C>G GRCh38
NC_000011.9:g.10350563C>G , CM000673.1:g.10350563C>G GRCh37
NC_000011.8:g.10307139C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000527261.5:n.362-1554C>G
ENST00000532250.5:c.-145-1554C>G ENSP00000432707.1:n.-145-1554C>G
NR_103765.1:n.362-1554C>G
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