Canonical Allele Identifier: CA1525691632
Gene: ADCY2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7617199A= , CM000667.2:g.7617199A= GRCh38
NC_000005.9:g.7617312A= , CM000667.1:g.7617312A= GRCh37
NC_000005.8:g.7670312A= NCBI36
NG_046913.1:g.225970A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338316.9:c.571-8968A= MANE Select ENSP00000342952.4:n.571-8968A=
ENST00000338316.8:c.571-8968A= ENSP00000342952.4:n.571-8968A=
ENST00000498598.1:n.270-8968A=
ENST00000515681.1:c.-64+6024A= ENSP00000425069.1:n.-64+6024A=
ENST00000537121.5:c.566-8968A= ENSP00000444803.2:n.566-8968A=
NM_020546.2:c.571-8968A= NP_065433.2:n.571-8968A=
XM_011513942.1:c.571-8968A= XP_011512244.1:n.571-8968A=
XR_427657.2:n.585-8968A=
XM_011513942.2:c.571-8968A= XP_011512244.1:n.571-8968A=
XR_001741973.1:n.585-8968A=
XR_001741974.2:n.585-8968A=
NM_020546.3:c.571-8968A= MANE Select NP_065433.2:n.571-8968A=