Canonical Allele Identifier: CA7308327
Gene: GPR68 HGNC NCBI

Linked Data

dbSNP Id: rs554876233

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91234443G>A , CM000676.2:g.91234443G>A GRCh38
NC_000014.8:g.91700787G>A , CM000676.1:g.91700787G>A GRCh37
NC_000014.7:g.90770540G>A NCBI36
NG_052988.1:g.24438C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000650645.1:c.608C>T MANE Select ENSP00000498702.1:p.Ala203Val
ENST00000529102.1:c.608C>T ENSP00000432740.1:p.Ala203Val
ENST00000531499.2:c.608C>T ENSP00000434045.2:p.Ala203Val
ENST00000535815.5:c.608C>T ENSP00000440797.1:p.Ala203Val
NM_001177676.1:c.608C>T NP_001171147.1:p.Ala203Val
NM_003485.3:c.608C>T NP_003476.3:p.Ala203Val
XM_005268110.3:c.638C>T XP_005268167.1:p.Ala213Val
XM_005268111.2:c.638C>T XP_005268168.1:p.Ala213Val
XM_005268112.2:c.638C>T XP_005268169.1:p.Ala213Val
XM_006720262.2:c.638C>T XP_006720325.1:p.Ala213Val
XM_011537196.1:c.638C>T XP_011535498.1:p.Ala213Val
XM_011537197.1:c.638C>T XP_011535499.1:p.Ala213Val
XM_011537198.1:c.638C>T XP_011535500.1:p.Ala213Val
XM_011537199.1:c.638C>T XP_011535501.1:p.Ala213Val
XM_011537200.1:c.638C>T XP_011535502.1:p.Ala213Val
NM_001348437.1:c.608C>T NP_001335366.1:p.Ala203Val
XM_005268110.4:c.638C>T XP_005268167.1:p.Ala213Val
XM_005268111.3:c.638C>T XP_005268168.1:p.Ala213Val
XM_005268112.3:c.638C>T XP_005268169.1:p.Ala213Val
XM_006720262.3:c.638C>T XP_006720325.1:p.Ala213Val
XM_011537196.2:c.638C>T XP_011535498.1:p.Ala213Val
XM_011537197.3:c.638C>T XP_011535499.1:p.Ala213Val
XM_011537198.2:c.638C>T XP_011535500.1:p.Ala213Val
XM_011537199.2:c.638C>T XP_011535501.1:p.Ala213Val
NM_001177676.2:c.608C>T MANE Select NP_001171147.1:p.Ala203Val