Canonical Allele Identifier: CA1549806482

Linked Data

dbSNP Id: rs181709466

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60491911G>C , CM000667.2:g.60491911G>C GRCh38
NC_000005.9:g.59787738G>C , CM000667.1:g.59787738G>C GRCh37
NC_000005.8:g.59823495G>C NCBI36
NG_027957.1:g.1188C>G
NG_027957.2:g.37419C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000506510.6:n.70+30140C>G (PDE4D)
NR_024617.1:n.711+3488G>C (PART1)
NR_028509.1:n.492+3488G>C (PART1)
XM_011543472.1:c.-90+30140C>G (PDE4D) XP_011541774.1:n.-90+30140C>G
NM_001364599.1:c.-90+4228C>G (PDE4D) NP_001351528.1:n.-90+4228C>G
XM_024446110.1:c.-90+30140C>G (PDE4D) XP_024301878.1:n.-90+30140C>G
XM_024446112.1:c.-90+30140C>G (PDE4D) XP_024301880.1:n.-90+30140C>G