Canonical Allele Identifier: CA2617795869
Gene: PDE6H HGNC NCBI

Linked Data

gnomAD v4: 12-14977898-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14977898T>C , CM000674.2:g.14977898T>C GRCh38
NC_000012.11:g.15130832T>C , CM000674.1:g.15130832T>C GRCh37
NC_000012.10:g.15022099T>C NCBI36
NG_016859.1:g.9877T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000266395.3:c.-41-74T>C MANE Select ENSP00000266395.2:n.-41-74T>C
ENST00000266395.2:c.-41-74T>C ENSP00000266395.2:n.-41-74T>C
NM_006205.2:c.-41-74T>C NP_006196.1:n.-41-74T>C
XR_931376.1:n.175+11589A>G
XM_017019431.2:c.-115T>C XP_016874920.1:n.-115T>C
XR_931376.2:n.389+11589A>G
NM_006205.3:c.-41-74T>C MANE Select NP_006196.1:n.-41-74T>C
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