Canonical Allele Identifier: CA149000089
Gene: ADGRG6 HGNC NCBI

Linked Data

dbSNP Id: rs3817928

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.142429379A>G , CM000668.2:g.142429379A>G GRCh38
NC_000006.11:g.142750516A>G , CM000668.1:g.142750516A>G GRCh37
NC_000006.10:g.142792209A>G NCBI36
NG_011839.1:g.132461A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000296932.13:c.3236-8055A>G ENSP00000296932.8:n.3236-8055A>G
ENST00000367609.8:c.3320-8055A>G MANE Select ENSP00000356581.3:n.3320-8055A>G
ENST00000230173.10:c.3320-8055A>G ENSP00000230173.6:n.3320-8055A>G
ENST00000296932.12:c.3236-8055A>G ENSP00000296932.8:n.3236-8055A>G
ENST00000367608.6:c.3236-8055A>G ENSP00000356580.2:n.3236-8055A>G
ENST00000367609.7:c.3320-8055A>G ENSP00000356581.3:n.3320-8055A>G
ENST00000472054.2:n.546-8055A>G
NM_001032394.2:c.3236-8055A>G NP_001027566.1:n.3236-8055A>G
NM_001032395.2:c.3236-8055A>G NP_001027567.1:n.3236-8055A>G
NM_020455.5:c.3320-8055A>G NP_065188.4:n.3320-8055A>G
NM_198569.2:c.3320-8055A>G NP_940971.1:n.3320-8055A>G
XM_005267061.2:c.3323-8055A>G XP_005267118.1:n.3323-8055A>G
XM_006715516.2:c.3323-8055A>G XP_006715579.1:n.3323-8055A>G
XM_006715517.2:c.3317-8055A>G XP_006715580.1:n.3317-8055A>G
XM_006715518.2:c.3239-8055A>G XP_006715581.1:n.3239-8055A>G
XM_011535964.1:c.3320-8055A>G XP_011534266.1:n.3320-8055A>G
XM_005267061.3:c.3323-8055A>G XP_005267118.1:n.3323-8055A>G
NM_198569.3:c.3320-8055A>G MANE Select NP_940971.2:n.3320-8055A>G
NM_001032394.3:c.3236-8055A>G NP_001027566.2:n.3236-8055A>G
NM_001032395.3:c.3236-8055A>G NP_001027567.2:n.3236-8055A>G
NM_020455.6:c.3320-8055A>G NP_065188.5:n.3320-8055A>G