Canonical Allele Identifier: CA2718238077
Gene: ADCY8 HGNC NCBI

Linked Data

dbSNP Id: rs2130091485

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.130795754G>A , CM000670.2:g.130795754G>A GRCh38
NC_000008.10:g.131808000G>A , CM000670.1:g.131808000G>A GRCh37
NC_000008.9:g.131877182G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286355.10:c.3060+4672C>T MANE Select ENSP00000286355.5:n.3060+4672C>T
ENST00000286355.9:c.3060+4672C>T ENSP00000286355.5:n.3060+4672C>T
ENST00000377928.7:c.2667+4672C>T ENSP00000367161.3:n.2667+4672C>T
NM_001115.2:c.3060+4672C>T NP_001106.1:n.3060+4672C>T
XM_005250769.2:c.2970+4672C>T XP_005250826.1:n.2970+4672C>T
XM_006716501.2:c.2862+4672C>T XP_006716564.1:n.2862+4672C>T
XM_005250769.3:c.2970+4672C>T XP_005250826.1:n.2970+4672C>T
XM_006716501.3:c.2862+4672C>T XP_006716564.1:n.2862+4672C>T
XM_017013006.1:c.2772+4672C>T XP_016868495.1:n.2772+4672C>T
NM_001115.3:c.3060+4672C>T MANE Select NP_001106.1:n.3060+4672C>T