Canonical Allele Identifier: CA341392079
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539555G>T , CM000663.2:g.100539555G>T GRCh38
NC_000001.10:g.101005111G>T , CM000663.1:g.101005111G>T GRCh37
NC_000001.9:g.100777699G>T NCBI36
NG_053134.1:g.6384G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.589G>T MANE Select ENSP00000314223.4:p.Ala197Ser
ENST00000315033.4:c.589G>T ENSP00000314223.4:p.Ala197Ser
NM_022049.2:c.589G>T NP_071332.2:p.Ala197Ser
NM_022049.3:c.589G>T MANE Select NP_071332.2:p.Ala197Ser