Canonical Allele Identifier: CA2723066055
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs142123436
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10369130C>A , CM000673.2:g.10369130C>A GRCh38
NC_000011.9:g.10390677C>A , CM000673.1:g.10390677C>A GRCh37
NC_000011.8:g.10347253C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295663.9:n.51-23152C>A
ENST00000527261.5:n.501+38421C>A
ENST00000532250.5:c.-6+38421C>A ENSP00000432707.1:n.-6+38421C>A
ENST00000532966.1:n.119+11739C>A
NR_103765.1:n.501+38421C>A
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