Canonical Allele Identifier: CA13447149

Gene: GPR83

Linked Data

• dbSNP Id: rs3758785
• gnomAD v2: 11-94132139-A-G
• gnomAD v3: 11-94398973-A-G
• gnomAD v4: 11-94398973-A-G
• MyVariant Identifiers: chr11:g.94132139A>G (hg19) ; chr11:g.94398973A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94398973A>G , CM000673.2:g.94398973A>G	GRCh38
NC_000011.9:g.94132139A>G , CM000673.1:g.94132139A>G	GRCh37
NC_000011.8:g.93771787A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000243673.7:c.387+1888T>C MANE Select	ENSP00000243673.2:n.387+1888T>C
ENST00000243673.6:c.387+1888T>C	ENSP00000243673.2:n.387+1888T>C
ENST00000539203.2:c.387+1888T>C	ENSP00000441550.1:n.387+1888T>C
NM_016540.3:c.387+1888T>C	NP_057624.3:n.387+1888T>C
XM_011542559.1:c.387+1888T>C	XP_011540861.1:n.387+1888T>C
NM_001330345.1:c.387+1888T>C	NP_001317274.1:n.387+1888T>C
NM_016540.4:c.387+1888T>C MANE Select	NP_057624.3:n.387+1888T>C
NM_001330345.2:c.387+1888T>C	NP_001317274.1:n.387+1888T>C