Canonical Allele Identifier: CA415270028

Gene: GPR50

Linked Data

• dbSNP Id: rs2048713863
• MyVariant Identifiers: chrX:g.150349805A>G (hg19) ; chrX:g.151181333A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181333A>G , CM000685.2:g.151181333A>G	GRCh38
NC_000023.10:g.150349805A>G , CM000685.1:g.150349805A>G	GRCh37
NC_000023.9:g.150100463A>G	NCBI36
NG_016405.1:g.9750A>G
NG_016405.2:g.9750A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218316.4:c.1750A>G MANE Select	ENSP00000218316.3:p.Ile584Val
ENST00000218316.3:c.1750A>G	ENSP00000218316.3:p.Ile584Val
ENST00000617907.1:c.1744A>G	ENSP00000484496.1:p.Ile582Val
NM_004224.3:c.1750A>G MANE Select	NP_004215.2:p.Ile584Val
XM_011531216.1:c.1009A>G	XP_011529518.1:p.Ile337Val
XM_011531216.2:c.1009A>G	XP_011529518.1:p.Ile337Val