Canonical Allele Identifier: CA13612800
Gene: GPR162 HGNC NCBI

Linked Data

dbSNP Id: rs2071081
gnomAD v2: 12-6935631-A-C
gnomAD v3: 12-6826466-A-C
gnomAD v4: 12-6826466-A-C
MyVariant Identifiers: chr12:g.6935631A>C (hg19) chr12:g.6826466A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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