Canonical Allele Identifier: CA2591526578
Gene: AMPD3 HGNC NCBI

Linked Data

dbSNP Id: rs2133725391

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.10368973G>C , CM000673.2:g.10368973G>C GRCh38
NC_000011.9:g.10390520G>C , CM000673.1:g.10390520G>C GRCh37
NC_000011.8:g.10347096G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000295663.9:n.51-23309G>C
ENST00000527261.5:n.501+38264G>C
ENST00000532250.5:c.-6+38264G>C ENSP00000432707.1:n.-6+38264G>C
ENST00000532966.1:n.119+11582G>C
NR_103765.1:n.501+38264G>C