Canonical Allele Identifier: CA813935736

Gene: ADCY2

Linked Data

• dbSNP Id: rs148472182
• gnomAD v3: 5-7517350-T-A
• gnomAD v4: 5-7517350-T-A
• MyVariant Identifiers: chr5:g.7517463T>A (hg19) ; chr5:g.7517350T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7517350T>A , CM000667.2:g.7517350T>A	GRCh38
NC_000005.9:g.7517463T>A , CM000667.1:g.7517463T>A	GRCh37
NC_000005.8:g.7570463T>A	NCBI36
NG_046913.1:g.126121T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000338316.9:c.409-3388T>A MANE Select	ENSP00000342952.4:n.409-3388T>A
ENST00000338316.8:c.409-3388T>A	ENSP00000342952.4:n.409-3388T>A
ENST00000484965.5:n.143-3388T>A
ENST00000498598.1:n.108-3388T>A
ENST00000537121.5:c.409-3388T>A	ENSP00000444803.2:n.409-3388T>A
NM_020546.2:c.409-3388T>A	NP_065433.2:n.409-3388T>A
XM_011513942.1:c.409-3388T>A	XP_011512244.1:n.409-3388T>A
XR_427657.2:n.423-3388T>A
XM_011513942.2:c.409-3388T>A	XP_011512244.1:n.409-3388T>A
XR_001741973.1:n.423-3388T>A
XR_001741974.2:n.423-3388T>A
NM_020546.3:c.409-3388T>A MANE Select	NP_065433.2:n.409-3388T>A