Canonical Allele Identifier: CA443216838
Gene: ADCY2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.7520889C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7520776C>A , CM000667.2:g.7520776C>A GRCh38
NC_000005.9:g.7520889C>A , CM000667.1:g.7520889C>A GRCh37
NC_000005.8:g.7573889C>A NCBI36
NG_046913.1:g.129547C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338316.9:c.447C>A MANE Select ENSP00000342952.4:p.Thr149=
ENST00000338316.8:c.447C>A ENSP00000342952.4:p.Thr149=
ENST00000484965.5:n.181C>A
ENST00000498598.1:n.146C>A
ENST00000537121.5:c.447C>A ENSP00000444803.2:p.Thr149=
NM_020546.2:c.447C>A NP_065433.2:p.Thr149=
XM_011513942.1:c.447C>A XP_011512244.1:p.Thr149=
XR_427657.2:n.461C>A
XM_011513942.2:c.447C>A XP_011512244.1:p.Thr149=
XR_001741973.1:n.461C>A
XR_001741974.2:n.461C>A
NM_020546.3:c.447C>A MANE Select NP_065433.2:p.Thr149=