Canonical Allele Identifier: CA3492422

Gene: GPR151

Linked Data

• ClinVar Variation Id: 782100
• ClinVar RCV Id: RCV000963443 ; RCV001543424
• dbSNP Id: rs114285050
• ExAC: 5:145895394 G / A
• gnomAD v2: 5-145895394-G-A
• gnomAD v3: 5-146515831-G-A
• gnomAD v4: 5-146515831-G-A
• COSMIC: COSM390265
• MyVariant Identifiers: chr5:g.145895394G>A (hg19) ; chr5:g.146515831G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.146515831G>A , CM000667.2:g.146515831G>A	GRCh38
NC_000005.9:g.145895394G>A , CM000667.1:g.145895394G>A	GRCh37
NC_000005.8:g.145875587G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000311104.3:c.283C>T MANE Select	ENSP00000308733.2:p.Arg95Ter
ENST00000311104.2:c.283C>T	ENSP00000308733.2:p.Arg95Ter
NM_194251.2:c.283C>T	NP_919227.2:p.Arg95Ter
NM_194251.3:c.283C>T MANE Select	NP_919227.2:p.Arg95Ter