Canonical Allele Identifier: CA419188168
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005551C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539995C>T , CM000663.2:g.100539995C>T GRCh38
NC_000001.10:g.101005551C>T , CM000663.1:g.101005551C>T GRCh37
NC_000001.9:g.100778139C>T NCBI36
NG_053134.1:g.6824C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1029C>T MANE Select ENSP00000314223.4:p.Phe343=
ENST00000315033.4:c.1029C>T ENSP00000314223.4:p.Phe343=
NM_022049.2:c.1029C>T NP_071332.2:p.Phe343=
NM_022049.3:c.1029C>T MANE Select NP_071332.2:p.Phe343=
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