Canonical Allele Identifier: CA519131649
Gene: GPR50 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.150349783C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181311C>A , CM000685.2:g.151181311C>A GRCh38
NC_000023.10:g.150349783C>A , CM000685.1:g.150349783C>A GRCh37
NC_000023.9:g.150100441C>A NCBI36
NG_016405.1:g.9728C>A
NG_016405.2:g.9728C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1728C>A MANE Select ENSP00000218316.3:p.Ala576=
ENST00000218316.3:c.1728C>A ENSP00000218316.3:p.Ala576=
ENST00000617907.1:c.1722C>A ENSP00000484496.1:p.Ala574=
NM_004224.3:c.1728C>A MANE Select NP_004215.2:p.Ala576=
XM_011531216.1:c.987C>A XP_011529518.1:p.Ala329=
XM_011531216.2:c.987C>A XP_011529518.1:p.Ala329=
Search 100 bp 5'
Search 100 bp 3'