Canonical Allele Identifier: CA2676848878
Gene: GRM6 HGNC NCBI

Linked Data

gnomAD v4: 5-178995059-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178995059C>T , CM000667.2:g.178995059C>T GRCh38
NC_000005.9:g.178422060C>T , CM000667.1:g.178422060C>T GRCh37
NC_000005.8:g.178354666C>T NCBI36
NG_008105.1:g.5065G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.-16-99G>A MANE Select ENSP00000430767.1:n.-16-99G>A
ENST00000650031.1:c.-16-99G>A ENSP00000497110.1:n.-16-99G>A
ENST00000231188.9:c.-115G>A ENSP00000231188.5:n.-115G>A
ENST00000517717.1:c.-16-99G>A ENSP00000430767.1:n.-16-99G>A
NM_000843.3:c.-115G>A NP_000834.2:n.-115G>A
NM_000843.4:c.-16-99G>A MANE Select NP_000834.2:n.-16-99G>A
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