Canonical Allele Identifier: CA813935739

Gene: ADCY2

Linked Data

• dbSNP Id: rs750479150
• gnomAD v3: 5-7517352-G-T
• gnomAD v4: 5-7517352-G-T
• MyVariant Identifiers: chr5:g.7517465G>T (hg19) ; chr5:g.7517352G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7517352G>T , CM000667.2:g.7517352G>T	GRCh38
NC_000005.9:g.7517465G>T , CM000667.1:g.7517465G>T	GRCh37
NC_000005.8:g.7570465G>T	NCBI36
NG_046913.1:g.126123G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338316.9:c.409-3386G>T MANE Select	ENSP00000342952.4:n.409-3386G>T
ENST00000338316.8:c.409-3386G>T	ENSP00000342952.4:n.409-3386G>T
ENST00000484965.5:n.143-3386G>T
ENST00000498598.1:n.108-3386G>T
ENST00000537121.5:c.409-3386G>T	ENSP00000444803.2:n.409-3386G>T
NM_020546.2:c.409-3386G>T	NP_065433.2:n.409-3386G>T
XM_011513942.1:c.409-3386G>T	XP_011512244.1:n.409-3386G>T
XR_427657.2:n.423-3386G>T
XM_011513942.2:c.409-3386G>T	XP_011512244.1:n.409-3386G>T
XR_001741973.1:n.423-3386G>T
XR_001741974.2:n.423-3386G>T
NM_020546.3:c.409-3386G>T MANE Select	NP_065433.2:n.409-3386G>T