Canonical Allele Identifier: CA378355726
Gene: GRK5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.121086026A>C (hg19) chr10:g.119326514A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119326514A>C , CM000672.2:g.119326514A>C GRCh38
NC_000010.10:g.121086026A>C , CM000672.1:g.121086026A>C GRCh37
NC_000010.9:g.121076016A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392870.3:c.53-2A>C MANE Select ENSP00000376609.2:n.53-2A>C
ENST00000392870.2:c.53-2A>C ENSP00000376609.2:n.53-2A>C
NM_005308.2:c.53-2A>C NP_005299.1:n.53-2A>C
XM_005269707.1:c.53-2A>C XP_005269764.1:n.53-2A>C
XM_005269708.1:c.53-54301A>C XP_005269765.1:n.53-54301A>C
XM_005269707.2:c.53-2A>C XP_005269764.1:n.53-2A>C
NM_005308.3:c.53-2A>C MANE Select NP_005299.1:n.53-2A>C
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