Canonical Allele Identifier: CA362430166
Gene: GRM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.178416085T>G (hg19) chr5:g.178989084T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178989084T>G , CM000667.2:g.178989084T>G GRCh38
NC_000005.9:g.178416085T>G , CM000667.1:g.178416085T>G GRCh37
NC_000005.8:g.178348691T>G NCBI36
NG_008105.1:g.11040A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.1205A>C MANE Select ENSP00000430767.1:p.Gln402Pro
ENST00000650031.1:c.1205A>C ENSP00000497110.1:p.Gln402Pro
ENST00000231188.9:c.1205A>C ENSP00000231188.5:p.Gln402Pro
ENST00000517717.1:c.1205A>C ENSP00000430767.1:p.Gln402Pro
NM_000843.3:c.1205A>C NP_000834.2:p.Gln402Pro
XR_941310.1:n.1470-663T>G
NM_000843.4:c.1205A>C MANE Select NP_000834.2:p.Gln402Pro
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