Canonical Allele Identifier: CA114144527

Gene: ADCY2

Linked Data

• dbSNP Id: rs1004157458
• gnomAD v3: 5-7530724-C-T
• gnomAD v4: 5-7530724-C-T
• MyVariant Identifiers: chr5:g.7530837C>T (hg19) ; chr5:g.7530724C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7530724C>T , CM000667.2:g.7530724C>T	GRCh38
NC_000005.9:g.7530837C>T , CM000667.1:g.7530837C>T	GRCh37
NC_000005.8:g.7583837C>T	NCBI36
NG_046913.1:g.139495C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000338316.9:c.570+9825C>T MANE Select	ENSP00000342952.4:n.570+9825C>T
ENST00000338316.8:c.570+9825C>T	ENSP00000342952.4:n.570+9825C>T
ENST00000498598.1:n.269+9825C>T
ENST00000537121.5:c.565+9825C>T	ENSP00000444803.2:n.565+9825C>T
NM_020546.2:c.570+9825C>T	NP_065433.2:n.570+9825C>T
XM_011513942.1:c.570+9825C>T	XP_011512244.1:n.570+9825C>T
XR_427657.2:n.584+9825C>T
XM_011513942.2:c.570+9825C>T	XP_011512244.1:n.570+9825C>T
XR_001741973.1:n.584+9825C>T
XR_001741974.2:n.584+9825C>T
NM_020546.3:c.570+9825C>T MANE Select	NP_065433.2:n.570+9825C>T