Canonical Allele Identifier: CA412240461

Gene: P2RY8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.1465690G>C , CM000685.2:g.1465690G>C	GRCh38
NC_000023.10:g.1584583G>C , CM000685.1:g.1584583G>C	GRCh37
NC_000023.9:g.1544583G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381297.10:c.869C>G MANE Select	ENSP00000370697.4:p.Pro290Arg
ENST00000381297.9:c.869C>G	ENSP00000370697.4:p.Pro290Arg
XM_005274429.2:c.869C>G	XP_005274486.1:p.Pro290Arg
XM_005274429.3:c.869C>G	XP_005274486.1:p.Pro290Arg
XM_006724443.2:c.1436C>G	XP_006724506.2:p.Pro479Arg
XM_006724443.3:c.1436C>G	XP_006724506.2:p.Pro479Arg
XM_011546178.1:c.869C>G	XP_011544480.1:p.Pro290Arg
XM_011546178.2:c.869C>G	XP_011544480.1:p.Pro290Arg
XM_011546179.1:c.869C>G	XP_011544481.1:p.Pro290Arg
XM_011546179.2:c.869C>G	XP_011544481.1:p.Pro290Arg