Canonical Allele Identifier: CA2617795879
Gene: PDE6H HGNC NCBI

Linked Data

gnomAD v4: 12-14977902-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14977902A>G , CM000674.2:g.14977902A>G GRCh38
NC_000012.11:g.15130836A>G , CM000674.1:g.15130836A>G GRCh37
NC_000012.10:g.15022103A>G NCBI36
NG_016859.1:g.9881A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000266395.3:c.-41-70A>G MANE Select ENSP00000266395.2:n.-41-70A>G
ENST00000266395.2:c.-41-70A>G ENSP00000266395.2:n.-41-70A>G
NM_006205.2:c.-41-70A>G NP_006196.1:n.-41-70A>G
XR_931376.1:n.175+11585T>C
XM_017019431.2:c.-111A>G XP_016874920.1:n.-111A>G
XR_931376.2:n.389+11585T>C
NM_006205.3:c.-41-70A>G MANE Select NP_006196.1:n.-41-70A>G
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