Canonical Allele Identifier: CA133035589
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs894195844
gnomAD v3: 5-178995025-C-T
gnomAD v4: 5-178995025-C-T
MyVariant Identifiers: chr5:g.178422026C>T (hg19) chr5:g.178995025C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178995025C>T , CM000667.2:g.178995025C>T GRCh38
NC_000005.9:g.178422026C>T , CM000667.1:g.178422026C>T GRCh37
NC_000005.8:g.178354632C>T NCBI36
NG_008105.1:g.5099G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.-16-65G>A MANE Select ENSP00000430767.1:n.-16-65G>A
ENST00000650031.1:c.-16-65G>A ENSP00000497110.1:n.-16-65G>A
ENST00000231188.9:c.-81G>A ENSP00000231188.5:n.-81G>A
ENST00000517717.1:c.-16-65G>A ENSP00000430767.1:n.-16-65G>A
NM_000843.3:c.-81G>A NP_000834.2:n.-81G>A
NM_000843.4:c.-16-65G>A MANE Select NP_000834.2:n.-16-65G>A
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