Canonical Allele Identifier: CA1525712018
Gene: ADCY2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7649694A= , CM000667.2:g.7649694A= GRCh38
NC_000005.9:g.7649807A= , CM000667.1:g.7649807A= GRCh37
NC_000005.8:g.7702807A= NCBI36
NG_046913.1:g.258465A=

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.720+23378A= MANE Select ENSP00000342952.4:n.720+23378A=
ENST00000338316.8:c.720+23378A= ENSP00000342952.4:n.720+23378A=
ENST00000498598.1:n.420-8332A=
ENST00000515681.1:c.87+23378A= ENSP00000425069.1:n.87+23378A=
ENST00000537121.5:c.714+23378A= ENSP00000444803.2:n.714+23378A=
NM_020546.2:c.720+23378A= NP_065433.2:n.720+23378A=
XM_011513942.1:c.720+23378A= XP_011512244.1:n.720+23378A=
XR_427657.2:n.734+23378A=
XM_011513942.2:c.720+23378A= XP_011512244.1:n.720+23378A=
XR_001741973.1:n.734+23378A=
XR_001741974.2:n.734+23378A=
NM_020546.3:c.720+23378A= MANE Select NP_065433.2:n.720+23378A=