Canonical Allele Identifier: CA10540477
Gene: GPR50 HGNC NCBI

Linked Data

dbSNP Id: rs780093398
ExAC: X:150349785 G / A
gnomAD v2: X-150349785-G-A
MyVariant Identifiers: chrX:g.150349785G>A (hg19) chrX:g.151181313G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181313G>A , CM000685.2:g.151181313G>A GRCh38
NC_000023.10:g.150349785G>A , CM000685.1:g.150349785G>A GRCh37
NC_000023.9:g.150100443G>A NCBI36
NG_016405.1:g.9730G>A
NG_016405.2:g.9730G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1730G>A MANE Select ENSP00000218316.3:p.Ser577Asn
ENST00000218316.3:c.1730G>A ENSP00000218316.3:p.Ser577Asn
ENST00000617907.1:c.1724G>A ENSP00000484496.1:p.Ser575Asn
NM_004224.3:c.1730G>A MANE Select NP_004215.2:p.Ser577Asn
XM_011531216.1:c.989G>A XP_011529518.1:p.Ser330Asn
XM_011531216.2:c.989G>A XP_011529518.1:p.Ser330Asn
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