Canonical Allele Identifier: CA2707895056
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs34528234

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7530613_7530614dup , CM000667.2:g.7530613_7530614dup GRCh38
NC_000005.9:g.7530726_7530727dup , CM000667.1:g.7530726_7530727dup GRCh37
NC_000005.8:g.7583726_7583727dup NCBI36
NG_046913.1:g.139384_139385dup

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.570+9714_570+9715dup MANE Select ENSP00000342952.4:n.570+9714_570+9715dup
ENST00000338316.8:c.570+9714_570+9715dup ENSP00000342952.4:n.570+9714_570+9715dup
ENST00000498598.1:n.269+9714_269+9715dup
ENST00000537121.5:c.565+9714_565+9715dup ENSP00000444803.2:n.565+9714_565+9715dup
NM_020546.2:c.570+9714_570+9715dup NP_065433.2:n.570+9714_570+9715dup
XM_011513942.1:c.570+9714_570+9715dup XP_011512244.1:n.570+9714_570+9715dup
XR_427657.2:n.584+9714_584+9715dup
XM_011513942.2:c.570+9714_570+9715dup XP_011512244.1:n.570+9714_570+9715dup
XR_001741973.1:n.584+9714_584+9715dup
XR_001741974.2:n.584+9714_584+9715dup
NM_020546.3:c.570+9714_570+9715dup MANE Select NP_065433.2:n.570+9714_570+9715dup