Canonical Allele Identifier: CA16218138
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs1846681

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7530628A>G , CM000667.2:g.7530628A>G GRCh38
NC_000005.9:g.7530741A>G , CM000667.1:g.7530741A>G GRCh37
NC_000005.8:g.7583741A>G NCBI36
NG_046913.1:g.139399A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.570+9729A>G MANE Select ENSP00000342952.4:n.570+9729A>G
ENST00000338316.8:c.570+9729A>G ENSP00000342952.4:n.570+9729A>G
ENST00000498598.1:n.269+9729A>G
ENST00000537121.5:c.565+9729A>G ENSP00000444803.2:n.565+9729A>G
NM_020546.2:c.570+9729A>G NP_065433.2:n.570+9729A>G
XM_011513942.1:c.570+9729A>G XP_011512244.1:n.570+9729A>G
XR_427657.2:n.584+9729A>G
XM_011513942.2:c.570+9729A>G XP_011512244.1:n.570+9729A>G
XR_001741973.1:n.584+9729A>G
XR_001741974.2:n.584+9729A>G
NM_020546.3:c.570+9729A>G MANE Select NP_065433.2:n.570+9729A>G