Canonical Allele Identifier: CA148998918

Gene: ADGRG6

Linked Data

• dbSNP Id: rs921094048
• gnomAD v2: 6-142703878-T-C
• gnomAD v3: 6-142382741-T-C
• gnomAD v4: 6-142382741-T-C
• MyVariant Identifiers: chr6:g.142703878T>C (hg19) ; chr6:g.142382741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.142382741T>C , CM000668.2:g.142382741T>C	GRCh38
NC_000006.11:g.142703878T>C , CM000668.1:g.142703878T>C	GRCh37
NC_000006.10:g.142745571T>C	NCBI36
NG_011839.1:g.85823T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000296932.13:c.1138+722T>C	ENSP00000296932.8:n.1138+722T>C
ENST00000367609.8:c.1138+722T>C MANE Select	ENSP00000356581.3:n.1138+722T>C
ENST00000230173.10:c.1138+722T>C	ENSP00000230173.6:n.1138+722T>C
ENST00000296932.12:c.1138+722T>C	ENSP00000296932.8:n.1138+722T>C
ENST00000367608.6:c.1138+722T>C	ENSP00000356580.2:n.1138+722T>C
ENST00000367609.7:c.1138+722T>C	ENSP00000356581.3:n.1138+722T>C
NM_001032394.2:c.1138+722T>C	NP_001027566.1:n.1138+722T>C
NM_001032395.2:c.1138+722T>C	NP_001027567.1:n.1138+722T>C
NM_020455.5:c.1138+722T>C	NP_065188.4:n.1138+722T>C
NM_198569.2:c.1138+722T>C	NP_940971.1:n.1138+722T>C
XM_005267061.2:c.1141+722T>C	XP_005267118.1:n.1141+722T>C
XM_006715516.2:c.1141+722T>C	XP_006715579.1:n.1141+722T>C
XM_006715517.2:c.1135+722T>C	XP_006715580.1:n.1135+722T>C
XM_006715518.2:c.1141+722T>C	XP_006715581.1:n.1141+722T>C
XM_011535964.1:c.1138+722T>C	XP_011534266.1:n.1138+722T>C
XM_005267061.3:c.1141+722T>C	XP_005267118.1:n.1141+722T>C
XM_017011085.1:c.1141+722T>C	XP_016866574.1:n.1141+722T>C
NM_198569.3:c.1138+722T>C MANE Select	NP_940971.2:n.1138+722T>C
NM_001032394.3:c.1138+722T>C	NP_001027566.2:n.1138+722T>C
NM_001032395.3:c.1138+722T>C	NP_001027567.2:n.1138+722T>C
NM_020455.6:c.1138+722T>C	NP_065188.5:n.1138+722T>C