Canonical Allele Identifier: CA1525711992
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs1739014678

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7649657C>T , CM000667.2:g.7649657C>T GRCh38
NC_000005.9:g.7649770C>T , CM000667.1:g.7649770C>T GRCh37
NC_000005.8:g.7702770C>T NCBI36
NG_046913.1:g.258428C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.720+23341C>T MANE Select ENSP00000342952.4:n.720+23341C>T
ENST00000338316.8:c.720+23341C>T ENSP00000342952.4:n.720+23341C>T
ENST00000498598.1:n.420-8369C>T
ENST00000515681.1:c.87+23341C>T ENSP00000425069.1:n.87+23341C>T
ENST00000537121.5:c.714+23341C>T ENSP00000444803.2:n.714+23341C>T
NM_020546.2:c.720+23341C>T NP_065433.2:n.720+23341C>T
XM_011513942.1:c.720+23341C>T XP_011512244.1:n.720+23341C>T
XR_427657.2:n.734+23341C>T
XM_011513942.2:c.720+23341C>T XP_011512244.1:n.720+23341C>T
XR_001741973.1:n.734+23341C>T
XR_001741974.2:n.734+23341C>T
NM_020546.3:c.720+23341C>T MANE Select NP_065433.2:n.720+23341C>T