Canonical Allele Identifier: CA419317270
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539701-C-A
MyVariant Identifiers: chr1:g.101005257C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539701C>A , CM000663.2:g.100539701C>A GRCh38
NC_000001.10:g.101005257C>A , CM000663.1:g.101005257C>A GRCh37
NC_000001.9:g.100777845C>A NCBI36
NG_053134.1:g.6530C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.735C>A MANE Select ENSP00000314223.4:p.Ala245=
ENST00000315033.4:c.735C>A ENSP00000314223.4:p.Ala245=
NM_022049.2:c.735C>A NP_071332.2:p.Ala245=
NM_022049.3:c.735C>A MANE Select NP_071332.2:p.Ala245=
Search 100 bp 5'
Search 100 bp 3'