Canonical Allele Identifier: CA1525711991
Gene: ADCY2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7649657C= , CM000667.2:g.7649657C= GRCh38
NC_000005.9:g.7649770C= , CM000667.1:g.7649770C= GRCh37
NC_000005.8:g.7702770C= NCBI36
NG_046913.1:g.258428C=

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.720+23341C= MANE Select ENSP00000342952.4:n.720+23341C=
ENST00000338316.8:c.720+23341C= ENSP00000342952.4:n.720+23341C=
ENST00000498598.1:n.420-8369C=
ENST00000515681.1:c.87+23341C= ENSP00000425069.1:n.87+23341C=
ENST00000537121.5:c.714+23341C= ENSP00000444803.2:n.714+23341C=
NM_020546.2:c.720+23341C= NP_065433.2:n.720+23341C=
XM_011513942.1:c.720+23341C= XP_011512244.1:n.720+23341C=
XR_427657.2:n.734+23341C=
XM_011513942.2:c.720+23341C= XP_011512244.1:n.720+23341C=
XR_001741973.1:n.734+23341C=
XR_001741974.2:n.734+23341C=
NM_020546.3:c.720+23341C= MANE Select NP_065433.2:n.720+23341C=