Canonical Allele Identifier: CA820016222

Gene: ADGRG6

Linked Data

• dbSNP Id: rs1250410194
• gnomAD v3: 6-142444187-A-G
• gnomAD v4: 6-142444187-A-G
• MyVariant Identifiers: chr6:g.142765324A>G (hg19) ; chr6:g.142444187A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142444187A>G , CM000668.2:g.142444187A>G	GRCh38
NC_000006.11:g.142765324A>G , CM000668.1:g.142765324A>G	GRCh37
NC_000006.10:g.142807017A>G	NCBI36
NG_011839.1:g.147269A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296932.13:c.*805A>G	ENSP00000296932.8:n.*805A>G
ENST00000367609.8:c.*672A>G MANE Select	ENSP00000356581.3:n.*672A>G
ENST00000230173.10:c.*805A>G	ENSP00000230173.6:n.*805A>G
ENST00000296932.12:c.*805A>G	ENSP00000296932.8:n.*805A>G
ENST00000367608.6:c.*672A>G	ENSP00000356580.2:n.*672A>G
ENST00000367609.7:c.*672A>G	ENSP00000356581.3:n.*672A>G
NM_001032394.2:c.*805A>G	NP_001027566.1:n.*805A>G
NM_001032395.2:c.*672A>G	NP_001027567.1:n.*672A>G
NM_020455.5:c.*805A>G	NP_065188.4:n.*805A>G
NM_198569.2:c.*672A>G	NP_940971.1:n.*672A>G
XM_005267061.2:c.*805A>G	XP_005267118.1:n.*805A>G
XM_006715516.2:c.*672A>G	XP_006715579.1:n.*672A>G
XM_006715517.2:c.*672A>G	XP_006715580.1:n.*672A>G
XM_006715518.2:c.*672A>G	XP_006715581.1:n.*672A>G
XM_011535964.1:c.*672A>G	XP_011534266.1:n.*672A>G
XM_005267061.3:c.*805A>G	XP_005267118.1:n.*805A>G
NM_198569.3:c.*672A>G MANE Select	NP_940971.2:n.*672A>G
NM_001032394.3:c.*805A>G	NP_001027566.2:n.*805A>G
NM_001032395.3:c.*672A>G	NP_001027567.2:n.*672A>G
NM_020455.6:c.*805A>G	NP_065188.5:n.*805A>G