Canonical Allele Identifier: CA419188109
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005470A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539914A>T , CM000663.2:g.100539914A>T GRCh38
NC_000001.10:g.101005470A>T , CM000663.1:g.101005470A>T GRCh37
NC_000001.9:g.100778058A>T NCBI36
NG_053134.1:g.6743A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.948A>T MANE Select ENSP00000314223.4:p.Gly316=
ENST00000315033.4:c.948A>T ENSP00000314223.4:p.Gly316=
NM_022049.2:c.948A>T NP_071332.2:p.Gly316=
NM_022049.3:c.948A>T MANE Select NP_071332.2:p.Gly316=
Search 100 bp 5'
Search 100 bp 3'