Canonical Allele Identifier: CA419317230
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005239C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539683C>G , CM000663.2:g.100539683C>G GRCh38
NC_000001.10:g.101005239C>G , CM000663.1:g.101005239C>G GRCh37
NC_000001.9:g.100777827C>G NCBI36
NG_053134.1:g.6512C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.717C>G MANE Select ENSP00000314223.4:p.Gly239=
ENST00000315033.4:c.717C>G ENSP00000314223.4:p.Gly239=
NM_022049.2:c.717C>G NP_071332.2:p.Gly239=
NM_022049.3:c.717C>G MANE Select NP_071332.2:p.Gly239=
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Search 100 bp 3'