Canonical Allele Identifier: CA596463427
Gene: GRK5 HGNC NCBI

Linked Data

dbSNP Id: rs1018535861
gnomAD v2: 10-121085997-C-G
gnomAD v4: 10-119326485-C-G
MyVariant Identifiers: chr10:g.121085997C>G (hg19) chr10:g.119326485C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119326485C>G , CM000672.2:g.119326485C>G GRCh38
NC_000010.10:g.121085997C>G , CM000672.1:g.121085997C>G GRCh37
NC_000010.9:g.121075987C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000392870.3:c.53-31C>G MANE Select ENSP00000376609.2:n.53-31C>G
ENST00000392870.2:c.53-31C>G ENSP00000376609.2:n.53-31C>G
NM_005308.2:c.53-31C>G NP_005299.1:n.53-31C>G
XM_005269707.1:c.53-31C>G XP_005269764.1:n.53-31C>G
XM_005269708.1:c.53-54330C>G XP_005269765.1:n.53-54330C>G
XM_005269707.2:c.53-31C>G XP_005269764.1:n.53-31C>G
NM_005308.3:c.53-31C>G MANE Select NP_005299.1:n.53-31C>G
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