Canonical Allele Identifier: CA166497621

Gene: GRM8

Linked Data

• dbSNP Id: rs2188186
• gnomAD v2: 7-126637851-C-A
• gnomAD v3: 7-126997797-C-A
• gnomAD v4: 7-126997797-C-A
• MyVariant Identifiers: chr7:g.126637851C>A (hg19) ; chr7:g.126997797C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.126997797C>A , CM000669.2:g.126997797C>A	GRCh38
NC_000007.13:g.126637851C>A , CM000669.1:g.126637851C>A	GRCh37
NC_000007.12:g.126425087C>A	NCBI36
NG_029532.1:g.259578G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000358373.8:c.728-93114G>T	ENSP00000351142.3:n.728-93114G>T
ENST00000706915.1:c.728-93114G>T	ENSP00000516623.1:n.728-93114G>T
ENST00000706916.1:c.728-93114G>T	ENSP00000516624.1:n.728-93114G>T
ENST00000706917.1:c.728-93114G>T	ENSP00000516625.1:n.728-93114G>T
ENST00000339582.7:c.728-93114G>T MANE Select	ENSP00000344173.2:n.728-93114G>T
ENST00000339582.6:c.728-93114G>T	ENSP00000344173.2:n.728-93114G>T
ENST00000341617.7:c.728-93114G>T	ENSP00000345747.3:n.728-93114G>T
ENST00000358373.7:c.728-93114G>T	ENSP00000351142.3:n.728-93114G>T
ENST00000448250.6:n.270-93114G>T
ENST00000457830.1:c.728-93114G>T	ENSP00000415522.1:n.728-93114G>T
ENST00000472701.5:c.728-93114G>T	ENSP00000419832.1:n.728-93114G>T
ENST00000480995.5:n.445-93114G>T
NM_000845.2:c.728-93114G>T	NP_000836.2:n.728-93114G>T
NM_001127323.1:c.728-93114G>T	NP_001120795.1:n.728-93114G>T
NR_028041.1:n.1039-93114G>T
XM_006715938.2:c.728-93114G>T	XP_006716001.1:n.728-93114G>T
XM_011516091.1:c.728-93114G>T	XP_011514393.1:n.728-93114G>T
XM_011516092.1:c.728-93114G>T	XP_011514394.1:n.728-93114G>T
XM_011516093.1:c.728-93114G>T	XP_011514395.1:n.728-93114G>T
XM_011516094.1:c.245-93114G>T	XP_011514396.1:n.245-93114G>T
XM_011516095.1:c.146-93114G>T	XP_011514397.1:n.146-93114G>T
XM_011516096.1:c.113-93114G>T	XP_011514398.1:n.113-93114G>T
XM_011516097.1:c.113-93114G>T	XP_011514399.1:n.113-93114G>T
XM_011516098.1:c.113-93114G>T	XP_011514400.1:n.113-93114G>T
XM_011516099.1:c.113-93114G>T	XP_011514401.1:n.113-93114G>T
XM_011516100.1:c.113-93114G>T	XP_011514402.1:n.113-93114G>T
XM_011516101.1:c.113-93114G>T	XP_011514403.1:n.113-93114G>T
XM_011516102.1:c.113-93114G>T	XP_011514404.1:n.113-93114G>T
XM_011516103.1:c.-110-93114G>T	XP_011514405.1:n.-110-93114G>T
XM_011516105.1:c.-324-46796G>T	XP_011514407.1:n.-324-46796G>T
XM_011516106.1:c.-324-46796G>T	XP_011514408.1:n.-324-46796G>T
XM_011516107.1:c.-111+60182G>T	XP_011514409.1:n.-111+60182G>T
XM_006715938.4:c.728-93114G>T	XP_006716001.1:n.728-93114G>T
XM_011516091.2:c.728-93114G>T	XP_011514393.1:n.728-93114G>T
XM_011516092.3:c.728-93114G>T	XP_011514394.1:n.728-93114G>T
XM_011516095.2:c.146-93114G>T	XP_011514397.1:n.146-93114G>T
XM_011516101.2:c.113-93114G>T	XP_011514403.1:n.113-93114G>T
XM_011516102.2:c.113-93114G>T	XP_011514404.1:n.113-93114G>T
XM_011516103.2:c.-110-93114G>T	XP_011514405.1:n.-110-93114G>T
XM_017012074.1:c.728-93114G>T	XP_016867563.1:n.728-93114G>T
XM_017012075.1:c.113-93114G>T	XP_016867564.1:n.113-93114G>T
XM_017012076.1:c.113-93114G>T	XP_016867565.1:n.113-93114G>T
XM_017012077.1:c.113-93114G>T	XP_016867566.1:n.113-93114G>T
XM_017012078.1:c.113-93114G>T	XP_016867567.1:n.113-93114G>T
XM_017012079.1:c.113-93114G>T	XP_016867568.1:n.113-93114G>T
NM_000845.3:c.728-93114G>T MANE Select	NP_000836.2:n.728-93114G>T
NM_001371083.1:c.728-93114G>T	NP_001358012.1:n.728-93114G>T
NM_001371084.1:c.728-93114G>T	NP_001358013.1:n.728-93114G>T
NM_001371085.1:c.728-93114G>T	NP_001358014.1:n.728-93114G>T
NM_001371086.1:c.728-93114G>T	NP_001358015.1:n.728-93114G>T
NM_001371087.1:c.113-93114G>T	NP_001358016.1:n.113-93114G>T
NM_001371088.1:c.728-93114G>T	NP_001358017.1:n.728-93114G>T
NR_163849.1:n.1184-93114G>T
NR_163850.1:n.363-93114G>T