Canonical Allele Identifier: CA12257054
Gene: PDE10A HGNC NCBI

Linked Data

dbSNP Id: rs9364813
gnomAD v2: 6-166128638-G-A
gnomAD v3: 6-165715150-G-A
gnomAD v4: 6-165715150-G-A
MyVariant Identifiers: chr6:g.166128638G>A (hg19) chr6:g.165715150G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.165715150G>A , CM000668.2:g.165715150G>A GRCh38
NC_000006.11:g.166128638G>A , CM000668.1:g.166128638G>A GRCh37
NC_000006.10:g.166048628G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000366882.7:c.-614-171582C>T ENSP00000355847.3:n.-614-171582C>T
ENST00000685292.1:n.572-3997C>T
ENST00000647768.3:c.107-3997C>T ENSP00000497930.3:n.107-3997C>T
ENST00000649882.1:n.551-3997C>T
ENST00000672859.1:c.-17-3997C>T ENSP00000500900.1:n.-17-3997C>T
ENST00000672902.1:c.-17-3997C>T ENSP00000500351.1:n.-17-3997C>T
ENST00000676766.1:c.107-171582C>T ENSP00000504611.1:n.107-171582C>T
ENST00000678161.1:c.-17-3997C>T ENSP00000503721.1:n.-17-3997C>T
ENST00000580695.1:n.497-171582C>T
XM_011535387.3:c.59-3997C>T XP_011533689.2:n.59-3997C>T
XM_017010194.2:c.59-3997C>T XP_016865683.1:n.59-3997C>T
XM_017010197.2:c.59-3997C>T XP_016865686.1:n.59-3997C>T
XR_001743121.2:n.2134-3997C>T
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