Canonical Allele Identifier: CA21265753
Gene: GRIK3 HGNC NCBI

Linked Data

dbSNP Id: rs942855276
gnomAD v3: 1-36820776-T-C
gnomAD v4: 1-36820776-T-C
MyVariant Identifiers: chr1:g.37286377T>C (hg19) chr1:g.36820776T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.36820776T>C , CM000663.2:g.36820776T>C GRCh38
NC_000001.10:g.37286377T>C , CM000663.1:g.37286377T>C GRCh37
NC_000001.9:g.37058964T>C NCBI36
NG_011447.1:g.218468A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373091.8:c.1755-922A>G MANE Select ENSP00000362183.3:n.1755-922A>G
ENST00000373091.7:c.1755-922A>G ENSP00000362183.3:n.1755-922A>G
ENST00000373093.4:c.1755-922A>G ENSP00000362185.4:n.1755-922A>G
NM_000831.3:c.1755-922A>G NP_000822.2:n.1755-922A>G
XM_011541295.1:c.660-922A>G XP_011539597.1:n.660-922A>G
NM_000831.4:c.1755-922A>G MANE Select NP_000822.2:n.1755-922A>G
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