Canonical Allele Identifier: CA915948393

Gene: ADCY6

Linked Data

• ClinVar Variation Id: 727707
• ClinVar RCV Id: RCV000902084
• dbSNP Id: rs1592154392

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.48770979C>T , CM000674.2:g.48770979C>T	GRCh38
NC_000012.11:g.49164762C>T , CM000674.1:g.49164762C>T	GRCh37
NC_000012.10:g.47451029C>T	NCBI36
NG_042166.1:g.23118G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357869.8:c.3052-9G>A MANE Select	ENSP00000350536.4:n.3052-9G>A
ENST00000307885.4:c.3052-9G>A	ENSP00000311405.4:n.3052-9G>A
ENST00000357869.7:c.2893-9G>A	ENSP00000350536.3:n.2893-9G>A
ENST00000547260.5:n.1897G>A
ENST00000550422.5:c.2893-9G>A	ENSP00000446730.1:n.2893-9G>A
NM_015270.3:c.3052-9G>A	NP_056085.1:n.3052-9G>A
NM_015270.4:c.3052-9G>A	NP_056085.1:n.3052-9G>A
NM_020983.2:c.2893-9G>A	NP_066193.1:n.2893-9G>A
XM_006719210.2:c.3052-9G>A	XP_006719273.1:n.3052-9G>A
XM_011537810.1:c.2749-9G>A	XP_011536112.1:n.2749-9G>A
XM_011537811.1:c.2590-9G>A	XP_011536113.1:n.2590-9G>A
XR_944483.1:n.3089-9G>A
XM_006719210.4:c.3052-9G>A	XP_006719273.1:n.3052-9G>A
XM_017018743.1:c.2749-9G>A	XP_016874232.1:n.2749-9G>A
XR_001748565.1:n.3510-9G>A
NM_015270.5:c.3052-9G>A MANE Select	NP_056085.1:n.3052-9G>A
NM_001390830.1:c.2893-9G>A	NP_001377759.1:n.2893-9G>A
NM_001390831.1:c.3052-9G>A	NP_001377760.1:n.3052-9G>A