Canonical Allele Identifier: CA148998916
Gene: ADGRG6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4896582

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.142382740G>A , CM000668.2:g.142382740G>A GRCh38
NC_000006.11:g.142703877G>A , CM000668.1:g.142703877G>A GRCh37
NC_000006.10:g.142745570G>A NCBI36
NG_011839.1:g.85822G>A

Transcript Alleles

HGVS Amino-acid change
NM_001032394.2:c.1138+721G>A VV NP_001027566.1:p.=
NM_001032395.2:c.1138+721G>A VV NP_001027567.1:p.=
NM_020455.5:c.1138+721G>A VV NP_065188.4:p.=
NM_198569.2:c.1138+721G>A VV NP_940971.1:p.=
XM_005267061.2:c.1141+721G>A XP_005267118.1:p.=
XM_006715516.2:c.1141+721G>A XP_006715579.1:p.=
XM_006715517.2:c.1135+721G>A XP_006715580.1:p.=
XM_006715518.2:c.1141+721G>A XP_006715581.1:p.=
XM_011535964.1:c.1138+721G>A XP_011534266.1:p.=
XM_005267061.3:c.1141+721G>A XP_005267118.1:p.=
XM_017011085.1:c.1141+721G>A XP_016866574.1:p.=
ENST00000230173.10:c.1138+721G>A ENSP00000230173.6:p.=
ENST00000296932.12:c.1138+721G>A ENSP00000296932.8:p.=
ENST00000367608.6:c.1138+721G>A ENSP00000356580.2:p.=
ENST00000367609.7:c.1138+721G>A ENSP00000356581.3:p.=