Canonical Allele Identifier: CA935071867
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs1964912493
gnomAD v3: 11-10329070-T-A
gnomAD v4: 11-10329070-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10329070T>A , CM000673.2:g.10329070T>A GRCh38
NC_000011.9:g.10350617T>A , CM000673.1:g.10350617T>A GRCh37
NC_000011.8:g.10307193T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000527261.5:n.362-1500T>A
ENST00000532250.5:c.-145-1500T>A ENSP00000432707.1:n.-145-1500T>A
NR_103765.1:n.362-1500T>A
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