Canonical Allele Identifier: CA11994665
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs17826816
gnomAD v2: 5-7519298-A-G
gnomAD v3: 5-7519185-A-G
gnomAD v4: 5-7519185-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7519185A>G , CM000667.2:g.7519185A>G GRCh38
NC_000005.9:g.7519298A>G , CM000667.1:g.7519298A>G GRCh37
NC_000005.8:g.7572298A>G NCBI36
NG_046913.1:g.127956A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.409-1553A>G MANE Select ENSP00000342952.4:n.409-1553A>G
ENST00000338316.8:c.409-1553A>G ENSP00000342952.4:n.409-1553A>G
ENST00000484965.5:n.143-1553A>G
ENST00000498598.1:n.108-1553A>G
ENST00000537121.5:c.409-1553A>G ENSP00000444803.2:n.409-1553A>G
NM_020546.2:c.409-1553A>G NP_065433.2:n.409-1553A>G
XM_011513942.1:c.409-1553A>G XP_011512244.1:n.409-1553A>G
XR_427657.2:n.423-1553A>G
XM_011513942.2:c.409-1553A>G XP_011512244.1:n.409-1553A>G
XR_001741973.1:n.423-1553A>G
XR_001741974.2:n.423-1553A>G
NM_020546.3:c.409-1553A>G MANE Select NP_065433.2:n.409-1553A>G