Canonical Allele Identifier: CA670948154
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs1249833080
MyVariant Identifiers: chr11:g.10390673A>G (hg19) chr11:g.10369126A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10369126A>G , CM000673.2:g.10369126A>G GRCh38
NC_000011.9:g.10390673A>G , CM000673.1:g.10390673A>G GRCh37
NC_000011.8:g.10347249A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295663.9:n.51-23156A>G
ENST00000527261.5:n.501+38417A>G
ENST00000532250.5:c.-6+38417A>G ENSP00000432707.1:n.-6+38417A>G
ENST00000532966.1:n.119+11735A>G
NR_103765.1:n.501+38417A>G
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