Canonical Allele Identifier: CA6465829
Gene: PDE6H HGNC NCBI

Linked Data

dbSNP Id: rs200829414
ExAC: 12:15130936 G / C
gnomAD v2: 12-15130936-G-C
gnomAD v3: 12-14978002-G-C
gnomAD v4: 12-14978002-G-C
MyVariant Identifiers: chr12:g.15130936G>C (hg19) chr12:g.14978002G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.14978002G>C , CM000674.2:g.14978002G>C GRCh38
NC_000012.11:g.15130936G>C , CM000674.1:g.15130936G>C GRCh37
NC_000012.10:g.15022203G>C NCBI36
NG_016859.1:g.9981G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000266395.3:c.-11G>C MANE Select ENSP00000266395.2:n.-11G>C
ENST00000266395.2:c.-11G>C ENSP00000266395.2:n.-11G>C
NM_006205.2:c.-11G>C NP_006196.1:n.-11G>C
XR_931376.1:n.175+11485C>G
XM_017019431.2:c.-11G>C XP_016874920.1:n.-11G>C
XR_931376.2:n.389+11485C>G
NM_006205.3:c.-11G>C MANE Select NP_006196.1:n.-11G>C
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