Canonical Allele Identifier: CA575839388
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1453807660
gnomAD v2: 7-86445161-C-A
gnomAD v3: 7-86815845-C-A
gnomAD v4: 7-86815845-C-A
MyVariant Identifiers: chr7:g.86445161C>A (hg19) chr7:g.86815845C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815845C>A , CM000669.2:g.86815845C>A GRCh38
NC_000007.13:g.86445161C>A , CM000669.1:g.86445161C>A GRCh37
NC_000007.12:g.86283097C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22994C>A MANE Select ENSP00000355316.2:n.1325-22994C>A
ENST00000361669.6:c.1325-22994C>A ENSP00000355316.2:n.1325-22994C>A
ENST00000439827.1:c.1324+28729C>A ENSP00000398767.1:n.1324+28729C>A
NM_000840.2:c.1325-22994C>A NP_000831.2:n.1325-22994C>A
XM_011516088.1:c.1324+28729C>A XP_011514390.1:n.1324+28729C>A
XM_011516090.1:c.1325-17177C>A XP_011514392.1:n.1325-17177C>A
NM_001363522.1:c.1324+28729C>A NP_001350451.1:n.1324+28729C>A
NM_000840.3:c.1325-22994C>A MANE Select NP_000831.2:n.1325-22994C>A
NM_001363522.2:c.1324+28729C>A NP_001350451.1:n.1324+28729C>A
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