Canonical Allele Identifier: CA575839398
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs1240929682
gnomAD v2: 7-86445339-G-A
gnomAD v3: 7-86816023-G-A
gnomAD v4: 7-86816023-G-A
MyVariant Identifiers: chr7:g.86445339G>A (hg19) chr7:g.86816023G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86816023G>A , CM000669.2:g.86816023G>A GRCh38
NC_000007.13:g.86445339G>A , CM000669.1:g.86445339G>A GRCh37
NC_000007.12:g.86283275G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-22816G>A MANE Select ENSP00000355316.2:n.1325-22816G>A
ENST00000361669.6:c.1325-22816G>A ENSP00000355316.2:n.1325-22816G>A
ENST00000439827.1:c.1324+28907G>A ENSP00000398767.1:n.1324+28907G>A
NM_000840.2:c.1325-22816G>A NP_000831.2:n.1325-22816G>A
XM_011516088.1:c.1324+28907G>A XP_011514390.1:n.1324+28907G>A
XM_011516090.1:c.1325-16999G>A XP_011514392.1:n.1325-16999G>A
NM_001363522.1:c.1324+28907G>A NP_001350451.1:n.1324+28907G>A
NM_000840.3:c.1325-22816G>A MANE Select NP_000831.2:n.1325-22816G>A
NM_001363522.2:c.1324+28907G>A NP_001350451.1:n.1324+28907G>A
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