Canonical Allele Identifier: CA691207514
Gene: GPR162 HGNC NCBI

Linked Data

dbSNP Id: rs2071081
gnomAD v3: 12-6826466-A-G
gnomAD v4: 12-6826466-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6826466A>G , CM000674.2:g.6826466A>G GRCh38
NC_000012.11:g.6935631A>G , CM000674.1:g.6935631A>G GRCh37
NC_000012.10:g.6805892A>G NCBI36
NG_033740.1:g.3094A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000311268.8:c.1215+113A>G MANE Select ENSP00000311528.3:n.1215+113A>G
ENST00000311268.7:c.1215+113A>G ENSP00000311528.3:n.1215+113A>G
ENST00000382315.7:c.303+113A>G ENSP00000371752.3:n.303+113A>G
ENST00000428545.6:c.363+113A>G ENSP00000399670.2:n.363+113A>G
ENST00000545321.1:c.569+113A>G
NM_014449.1:c.363+113A>G NP_055264.1:n.363+113A>G
NM_019858.1:c.1215+113A>G NP_062832.1:n.1215+113A>G
NM_019858.2:c.1215+113A>G MANE Select NP_062832.1:n.1215+113A>G
NM_014449.2:c.363+113A>G NP_055264.1:n.363+113A>G