Canonical Allele Identifier: CA419317479
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005143G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539587G>C , CM000663.2:g.100539587G>C GRCh38
NC_000001.10:g.101005143G>C , CM000663.1:g.101005143G>C GRCh37
NC_000001.9:g.100777731G>C NCBI36
NG_053134.1:g.6416G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.621G>C MANE Select ENSP00000314223.4:p.Leu207=
ENST00000315033.4:c.621G>C ENSP00000314223.4:p.Leu207=
NM_022049.2:c.621G>C NP_071332.2:p.Leu207=
NM_022049.3:c.621G>C MANE Select NP_071332.2:p.Leu207=
Search 100 bp 5'
Search 100 bp 3'