Canonical Allele Identifier: CA415270019

Gene: GPR50

Linked Data

• dbSNP Id: rs2048713791
• gnomAD v4: X-151181328-A-G
• MyVariant Identifiers: chrX:g.150349800A>G (hg19) ; chrX:g.151181328A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.151181328A>G , CM000685.2:g.151181328A>G	GRCh38
NC_000023.10:g.150349800A>G , CM000685.1:g.150349800A>G	GRCh37
NC_000023.9:g.150100458A>G	NCBI36
NG_016405.1:g.9745A>G
NG_016405.2:g.9745A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218316.4:c.1745A>G MANE Select	ENSP00000218316.3:p.Asp582Gly
ENST00000218316.3:c.1745A>G	ENSP00000218316.3:p.Asp582Gly
ENST00000617907.1:c.1739A>G	ENSP00000484496.1:p.Asp580Gly
NM_004224.3:c.1745A>G MANE Select	NP_004215.2:p.Asp582Gly
XM_011531216.1:c.1004A>G	XP_011529518.1:p.Asp335Gly
XM_011531216.2:c.1004A>G	XP_011529518.1:p.Asp335Gly