Canonical Allele Identifier: CA519131716

Gene: GPR50

Linked Data

• dbSNP Id: rs2048714078
• MyVariant Identifiers: chrX:g.150349822C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181350C>T , CM000685.2:g.151181350C>T	GRCh38
NC_000023.10:g.150349822C>T , CM000685.1:g.150349822C>T	GRCh37
NC_000023.9:g.150100480C>T	NCBI36
NG_016405.1:g.9767C>T
NG_016405.2:g.9767C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218316.4:c.1767C>T MANE Select	ENSP00000218316.3:p.Asp589=
ENST00000218316.3:c.1767C>T	ENSP00000218316.3:p.Asp589=
ENST00000617907.1:c.1761C>T	ENSP00000484496.1:p.Asp587=
NM_004224.3:c.1767C>T MANE Select	NP_004215.2:p.Asp589=
XM_011531216.1:c.1026C>T	XP_011529518.1:p.Asp342=
XM_011531216.2:c.1026C>T	XP_011529518.1:p.Asp342=