Canonical Allele Identifier: CA843335766
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1479669185
MyVariant Identifiers: chr7:g.86445232A>G (hg19) chr7:g.86815916A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815916A>G , CM000669.2:g.86815916A>G GRCh38
NC_000007.13:g.86445232A>G , CM000669.1:g.86445232A>G GRCh37
NC_000007.12:g.86283168A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22923A>G MANE Select ENSP00000355316.2:n.1325-22923A>G
ENST00000361669.6:c.1325-22923A>G ENSP00000355316.2:n.1325-22923A>G
ENST00000439827.1:c.1324+28800A>G ENSP00000398767.1:n.1324+28800A>G
NM_000840.2:c.1325-22923A>G NP_000831.2:n.1325-22923A>G
XM_011516088.1:c.1324+28800A>G XP_011514390.1:n.1324+28800A>G
XM_011516090.1:c.1325-17106A>G XP_011514392.1:n.1325-17106A>G
NM_001363522.1:c.1324+28800A>G NP_001350451.1:n.1324+28800A>G
NM_000840.3:c.1325-22923A>G MANE Select NP_000831.2:n.1325-22923A>G
NM_001363522.2:c.1324+28800A>G NP_001350451.1:n.1324+28800A>G
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