Canonical Allele Identifier: CA6465859
Gene: PDE6H HGNC NCBI

Linked Data

dbSNP Id: rs779956922
ExAC: 12:15131089 A / G
gnomAD v2: 12-15131089-A-G
gnomAD v4: 12-14978155-A-G
MyVariant Identifiers: chr12:g.15131089A>G (hg19) chr12:g.14978155A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14978155A>G , CM000674.2:g.14978155A>G GRCh38
NC_000012.11:g.15131089A>G , CM000674.1:g.15131089A>G GRCh37
NC_000012.10:g.15022356A>G NCBI36
NG_016859.1:g.10134A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266395.3:c.134+9A>G MANE Select ENSP00000266395.2:n.134+9A>G
ENST00000266395.2:c.134+9A>G ENSP00000266395.2:n.134+9A>G
NM_006205.2:c.134+9A>G NP_006196.1:n.134+9A>G
XR_931376.1:n.175+11332T>C
XM_017019431.2:c.134+9A>G XP_016874920.1:n.134+9A>G
XR_931376.2:n.389+11332T>C
NM_006205.3:c.134+9A>G MANE Select NP_006196.1:n.134+9A>G
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