Canonical Allele Identifier: CA217931178
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs1039005163
MyVariant Identifiers: chr11:g.10350609C>G (hg19) chr11:g.10329062C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10329062C>G , CM000673.2:g.10329062C>G GRCh38
NC_000011.9:g.10350609C>G , CM000673.1:g.10350609C>G GRCh37
NC_000011.8:g.10307185C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000527261.5:n.362-1508C>G
ENST00000532250.5:c.-145-1508C>G ENSP00000432707.1:n.-145-1508C>G
NR_103765.1:n.362-1508C>G
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