Canonical Allele Identifier: CA16040620
Gene: GPR68 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 268086
dbSNP Id: rs1057517672

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.91234830A>G , CM000676.2:g.91234830A>G GRCh38
NC_000014.8:g.91701174A>G , CM000676.1:g.91701174A>G GRCh37
NC_000014.7:g.90770927A>G NCBI36
NG_052988.1:g.24051T>C

Transcript Alleles

HGVS Amino-acid change
NM_001177676.1:c.221T>C VV NP_001171147.1:p.Leu74Pro
NM_003485.3:c.221T>C VV NP_003476.3:p.Leu74Pro
XM_005268110.3:c.251T>C XP_005268167.1:p.Leu84Pro
XM_005268111.2:c.251T>C XP_005268168.1:p.Leu84Pro
XM_005268112.2:c.251T>C XP_005268169.1:p.Leu84Pro
XM_006720262.2:c.251T>C XP_006720325.1:p.Leu84Pro
XM_011537196.1:c.251T>C XP_011535498.1:p.Leu84Pro
XM_011537197.1:c.251T>C XP_011535499.1:p.Leu84Pro
XM_011537198.1:c.251T>C XP_011535500.1:p.Leu84Pro
XM_011537199.1:c.251T>C XP_011535501.1:p.Leu84Pro
XM_011537200.1:c.251T>C XP_011535502.1:p.Leu84Pro
NM_001348437.1:c.221T>C VV NP_001335366.1:p.Leu74Pro
XM_005268110.4:c.251T>C XP_005268167.1:p.Leu84Pro
XM_005268111.3:c.251T>C XP_005268168.1:p.Leu84Pro
XM_005268112.3:c.251T>C XP_005268169.1:p.Leu84Pro
XM_006720262.3:c.251T>C XP_006720325.1:p.Leu84Pro
XM_011537196.2:c.251T>C XP_011535498.1:p.Leu84Pro
XM_011537197.3:c.251T>C XP_011535499.1:p.Leu84Pro
XM_011537198.2:c.251T>C XP_011535500.1:p.Leu84Pro
XM_011537199.2:c.251T>C XP_011535501.1:p.Leu84Pro
NM_001177676.2:c.221T>C VV MANE Preferred NP_001171147.1:p.Leu74Pro
ENST00000529102.1:c.221T>C ENSP00000432740.1:p.Leu74Pro
ENST00000531499.2:c.221T>C ENSP00000434045.2:p.Leu74Pro
ENST00000535815.5:c.221T>C ENSP00000440797.1:p.Leu74Pro