Canonical Allele Identifier: CA843335789
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1359011392
gnomAD v3: 7-86816016-T-C
gnomAD v4: 7-86816016-T-C
MyVariant Identifiers: chr7:g.86445332T>C (hg19) chr7:g.86816016T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86816016T>C , CM000669.2:g.86816016T>C GRCh38
NC_000007.13:g.86445332T>C , CM000669.1:g.86445332T>C GRCh37
NC_000007.12:g.86283268T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22823T>C MANE Select ENSP00000355316.2:n.1325-22823T>C
ENST00000361669.6:c.1325-22823T>C ENSP00000355316.2:n.1325-22823T>C
ENST00000439827.1:c.1324+28900T>C ENSP00000398767.1:n.1324+28900T>C
NM_000840.2:c.1325-22823T>C NP_000831.2:n.1325-22823T>C
XM_011516088.1:c.1324+28900T>C XP_011514390.1:n.1324+28900T>C
XM_011516090.1:c.1325-17006T>C XP_011514392.1:n.1325-17006T>C
NM_001363522.1:c.1324+28900T>C NP_001350451.1:n.1324+28900T>C
NM_000840.3:c.1325-22823T>C MANE Select NP_000831.2:n.1325-22823T>C
NM_001363522.2:c.1324+28900T>C NP_001350451.1:n.1324+28900T>C
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