Canonical Allele Identifier: CA519131624
Gene: GPR50 HGNC NCBI

Linked Data

gnomAD v4: X-151181299-C-G
MyVariant Identifiers: chrX:g.150349771C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.151181299C>G , CM000685.2:g.151181299C>G GRCh38
NC_000023.10:g.150349771C>G , CM000685.1:g.150349771C>G GRCh37
NC_000023.9:g.150100429C>G NCBI36
NG_016405.1:g.9716C>G
NG_016405.2:g.9716C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000218316.4:c.1716C>G MANE Select ENSP00000218316.3:p.Thr572=
ENST00000218316.3:c.1716C>G ENSP00000218316.3:p.Thr572=
ENST00000617907.1:c.1710C>G ENSP00000484496.1:p.Thr570=
NM_004224.3:c.1716C>G MANE Select NP_004215.2:p.Thr572=
XM_011531216.1:c.975C>G XP_011529518.1:p.Thr325=
XM_011531216.2:c.975C>G XP_011529518.1:p.Thr325=
Search 100 bp 5'
Search 100 bp 3'