Canonical Allele Identifier: CA265533521

Gene: GPR68

Linked Data

• dbSNP Id: rs534616954
• gnomAD v2: 14-91700761-C-T
• gnomAD v3: 14-91234417-C-T
• gnomAD v4: 14-91234417-C-T
• MyVariant Identifiers: chr14:g.91700761C>T (hg19) ; chr14:g.91234417C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91234417C>T , CM000676.2:g.91234417C>T	GRCh38
NC_000014.8:g.91700761C>T , CM000676.1:g.91700761C>T	GRCh37
NC_000014.7:g.90770514C>T	NCBI36
NG_052988.1:g.24464G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650645.1:c.634G>A MANE Select	ENSP00000498702.1:p.Val212Met
ENST00000529102.1:c.634G>A	ENSP00000432740.1:p.Val212Met
ENST00000531499.2:c.634G>A	ENSP00000434045.2:p.Val212Met
ENST00000535815.5:c.634G>A	ENSP00000440797.1:p.Val212Met
NM_001177676.1:c.634G>A	NP_001171147.1:p.Val212Met
NM_003485.3:c.634G>A	NP_003476.3:p.Val212Met
XM_005268110.3:c.664G>A	XP_005268167.1:p.Val222Met
XM_005268111.2:c.664G>A	XP_005268168.1:p.Val222Met
XM_005268112.2:c.664G>A	XP_005268169.1:p.Val222Met
XM_006720262.2:c.664G>A	XP_006720325.1:p.Val222Met
XM_011537196.1:c.664G>A	XP_011535498.1:p.Val222Met
XM_011537197.1:c.664G>A	XP_011535499.1:p.Val222Met
XM_011537198.1:c.664G>A	XP_011535500.1:p.Val222Met
XM_011537199.1:c.664G>A	XP_011535501.1:p.Val222Met
XM_011537200.1:c.664G>A	XP_011535502.1:p.Val222Met
NM_001348437.1:c.634G>A	NP_001335366.1:p.Val212Met
XM_005268110.4:c.664G>A	XP_005268167.1:p.Val222Met
XM_005268111.3:c.664G>A	XP_005268168.1:p.Val222Met
XM_005268112.3:c.664G>A	XP_005268169.1:p.Val222Met
XM_006720262.3:c.664G>A	XP_006720325.1:p.Val222Met
XM_011537196.2:c.664G>A	XP_011535498.1:p.Val222Met
XM_011537197.3:c.664G>A	XP_011535499.1:p.Val222Met
XM_011537198.2:c.664G>A	XP_011535500.1:p.Val222Met
XM_011537199.2:c.664G>A	XP_011535501.1:p.Val222Met
NM_001177676.2:c.634G>A MANE Select	NP_001171147.1:p.Val212Met