Canonical Allele Identifier: CA575839371
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs959870874
gnomAD v2: 7-86444894-T-A
gnomAD v3: 7-86815578-T-A
gnomAD v4: 7-86815578-T-A
MyVariant Identifiers: chr7:g.86444894T>A (hg19) chr7:g.86815578T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86815578T>A , CM000669.2:g.86815578T>A GRCh38
NC_000007.13:g.86444894T>A , CM000669.1:g.86444894T>A GRCh37
NC_000007.12:g.86282830T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361669.7:c.1325-23261T>A MANE Select ENSP00000355316.2:n.1325-23261T>A
ENST00000361669.6:c.1325-23261T>A ENSP00000355316.2:n.1325-23261T>A
ENST00000439827.1:c.1324+28462T>A ENSP00000398767.1:n.1324+28462T>A
NM_000840.2:c.1325-23261T>A NP_000831.2:n.1325-23261T>A
XM_011516088.1:c.1324+28462T>A XP_011514390.1:n.1324+28462T>A
XM_011516090.1:c.1325-17444T>A XP_011514392.1:n.1325-17444T>A
NM_001363522.1:c.1324+28462T>A NP_001350451.1:n.1324+28462T>A
NM_000840.3:c.1325-23261T>A MANE Select NP_000831.2:n.1325-23261T>A
NM_001363522.2:c.1324+28462T>A NP_001350451.1:n.1324+28462T>A
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