Canonical Allele Identifier: CA217639851
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs909264729
gnomAD v3: 11-10369116-G-C
gnomAD v4: 11-10369116-G-C
MyVariant Identifiers: chr11:g.10390663G>C (hg19) chr11:g.10369116G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10369116G>C , CM000673.2:g.10369116G>C GRCh38
NC_000011.9:g.10390663G>C , CM000673.1:g.10390663G>C GRCh37
NC_000011.8:g.10347239G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295663.9:n.51-23166G>C
ENST00000527261.5:n.501+38407G>C
ENST00000532250.5:c.-6+38407G>C ENSP00000432707.1:n.-6+38407G>C
ENST00000532966.1:n.119+11725G>C
NR_103765.1:n.501+38407G>C
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