Canonical Allele Identifier: CA359164023

Gene: ADCY2

Linked Data

• gnomAD v4: 5-7520775-C-A
• MyVariant Identifiers: chr5:g.7520888C>A (hg19) ; chr5:g.7520775C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7520775C>A , CM000667.2:g.7520775C>A	GRCh38
NC_000005.9:g.7520888C>A , CM000667.1:g.7520888C>A	GRCh37
NC_000005.8:g.7573888C>A	NCBI36
NG_046913.1:g.129546C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338316.9:c.446C>A MANE Select	ENSP00000342952.4:p.Thr149Asn
ENST00000338316.8:c.446C>A	ENSP00000342952.4:p.Thr149Asn
ENST00000484965.5:n.180C>A
ENST00000498598.1:n.145C>A
ENST00000537121.5:c.446C>A	ENSP00000444803.2:p.Thr149Asn
NM_020546.2:c.446C>A	NP_065433.2:p.Thr149Asn
XM_011513942.1:c.446C>A	XP_011512244.1:p.Thr149Asn
XR_427657.2:n.460C>A
XM_011513942.2:c.446C>A	XP_011512244.1:p.Thr149Asn
XR_001741973.1:n.460C>A
XR_001741974.2:n.460C>A
NM_020546.3:c.446C>A MANE Select	NP_065433.2:p.Thr149Asn