Canonical Allele Identifier: CA133032052
Gene: GRM6 HGNC NCBI

Linked Data

ClinVar Variation Id: 849212
ClinVar RCV Id: RCV001053125 RCV002553307 RCV003938420
dbSNP Id: rs971140136
gnomAD v2: 5-178421531-G-T
gnomAD v3: 5-178994530-G-T
gnomAD v4: 5-178994530-G-T
MyVariant Identifiers: chr5:g.178421531G>T (hg19) chr5:g.178994530G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994530G>T , CM000667.2:g.178994530G>T GRCh38
NC_000005.9:g.178421531G>T , CM000667.1:g.178421531G>T GRCh37
NC_000005.8:g.178354137G>T NCBI36
NG_008105.1:g.5594C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.415C>A MANE Select ENSP00000430767.1:p.Pro139Thr
ENST00000650031.1:c.415C>A ENSP00000497110.1:p.Pro139Thr
ENST00000231188.9:c.415C>A ENSP00000231188.5:p.Pro139Thr
ENST00000517717.1:c.415C>A ENSP00000430767.1:p.Pro139Thr
NM_000843.3:c.415C>A NP_000834.2:p.Pro139Thr
NM_000843.4:c.415C>A MANE Select NP_000834.2:p.Pro139Thr
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Search 100 bp 3'