Canonical Allele Identifier: CA519128776
Gene: GPR50 HGNC NCBI
GPR50-AS1 HGNC NCBI

Linked Data

gnomAD v4: X-151177399-T-A
MyVariant Identifiers: chrX:g.150345871T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151177399T>A , CM000685.2:g.151177399T>A GRCh38
NC_000023.10:g.150345871T>A , CM000685.1:g.150345871T>A GRCh37
NC_000023.9:g.150096529T>A NCBI36
NG_016405.1:g.5816T>A
NG_016405.2:g.5816T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.187+491T>A (GPR50) MANE Select ENSP00000218316.3:n.187+491T>A
ENST00000218316.3:c.187+491T>A (GPR50) ENSP00000218316.3:n.187+491T>A
ENST00000617907.1:c.187+491T>A (GPR50) ENSP00000484496.1:n.187+491T>A
NM_004224.3:c.187+491T>A (GPR50) MANE Select NP_004215.2:n.187+491T>A
NR_135300.1:n.438A>T (GPR50-AS1)
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