Canonical Allele Identifier: CA847506430

Gene: ADCY8

Linked Data

• dbSNP Id: rs1307773676
• gnomAD v3: 8-130795824-C-T
• gnomAD v4: 8-130795824-C-T
• MyVariant Identifiers: chr8:g.131808070C>T (hg19) ; chr8:g.130795824C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.130795824C>T , CM000670.2:g.130795824C>T	GRCh38
NC_000008.10:g.131808070C>T , CM000670.1:g.131808070C>T	GRCh37
NC_000008.9:g.131877252C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000286355.10:c.3060+4602G>A MANE Select	ENSP00000286355.5:n.3060+4602G>A
ENST00000286355.9:c.3060+4602G>A	ENSP00000286355.5:n.3060+4602G>A
ENST00000377928.7:c.2667+4602G>A	ENSP00000367161.3:n.2667+4602G>A
NM_001115.2:c.3060+4602G>A	NP_001106.1:n.3060+4602G>A
XM_005250769.2:c.2970+4602G>A	XP_005250826.1:n.2970+4602G>A
XM_006716501.2:c.2862+4602G>A	XP_006716564.1:n.2862+4602G>A
XM_005250769.3:c.2970+4602G>A	XP_005250826.1:n.2970+4602G>A
XM_006716501.3:c.2862+4602G>A	XP_006716564.1:n.2862+4602G>A
XM_017013006.1:c.2772+4602G>A	XP_016868495.1:n.2772+4602G>A
NM_001115.3:c.3060+4602G>A MANE Select	NP_001106.1:n.3060+4602G>A