Canonical Allele Identifier: CA162445193
Gene: GRM3 HGNC NCBI

Linked Data

dbSNP Id: rs13242038
gnomAD v2: 7-86314420-C-T
gnomAD v3: 7-86685104-C-T
gnomAD v4: 7-86685104-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.86685104C>T , CM000669.2:g.86685104C>T GRCh38
NC_000007.13:g.86314420C>T , CM000669.1:g.86314420C>T GRCh37
NC_000007.12:g.86152356C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361669.7:c.-141+40232C>T MANE Select ENSP00000355316.2:n.-141+40232C>T
ENST00000361669.6:c.-141+40232C>T ENSP00000355316.2:n.-141+40232C>T
ENST00000421579.1:c.-141+40133C>T ENSP00000390037.1:n.-141+40133C>T
ENST00000439827.1:c.-141+40232C>T ENSP00000398767.1:n.-141+40232C>T
ENST00000454217.1:c.84+40232C>T ENSP00000405427.1:n.84+40232C>T
NM_000840.2:c.-141+40232C>T NP_000831.2:n.-141+40232C>T
XM_011516088.1:c.-141+40232C>T XP_011514390.1:n.-141+40232C>T
XM_011516089.1:c.-141+40232C>T XP_011514391.1:n.-141+40232C>T
XM_011516090.1:c.-141+40232C>T XP_011514392.1:n.-141+40232C>T
NM_001363522.1:c.-141+40232C>T NP_001350451.1:n.-141+40232C>T
XM_017012073.2:c.-141+40232C>T XP_016867562.1:n.-141+40232C>T
NM_000840.3:c.-141+40232C>T MANE Select NP_000831.2:n.-141+40232C>T
NM_001363522.2:c.-141+40232C>T NP_001350451.1:n.-141+40232C>T