Canonical Allele Identifier: CA3594152
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs775127730
ExAC: 5:178416080 C / A
gnomAD v2: 5-178416080-C-A
gnomAD v4: 5-178989079-C-A
MyVariant Identifiers: chr5:g.178416080C>A (hg19) chr5:g.178989079C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178989079C>A , CM000667.2:g.178989079C>A GRCh38
NC_000005.9:g.178416080C>A , CM000667.1:g.178416080C>A GRCh37
NC_000005.8:g.178348686C>A NCBI36
NG_008105.1:g.11045G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.1210G>T MANE Select ENSP00000430767.1:p.Val404Leu
ENST00000650031.1:c.1210G>T ENSP00000497110.1:p.Val404Leu
ENST00000231188.9:c.1210G>T ENSP00000231188.5:p.Val404Leu
ENST00000517717.1:c.1210G>T ENSP00000430767.1:p.Val404Leu
NM_000843.3:c.1210G>T NP_000834.2:p.Val404Leu
XR_941310.1:n.1470-668C>A
NM_000843.4:c.1210G>T MANE Select NP_000834.2:p.Val404Leu
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