Canonical Allele Identifier: CA362429947
Gene: GRM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.178415983G>T (hg19) chr5:g.178988982G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178988982G>T , CM000667.2:g.178988982G>T GRCh38
NC_000005.9:g.178415983G>T , CM000667.1:g.178415983G>T GRCh37
NC_000005.8:g.178348589G>T NCBI36
NG_008105.1:g.11142C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000517717.3:c.1307C>A MANE Select ENSP00000430767.1:p.Thr436Asn
ENST00000650031.1:c.1307C>A ENSP00000497110.1:p.Thr436Asn
ENST00000231188.9:c.1307C>A ENSP00000231188.5:p.Thr436Asn
ENST00000517717.1:c.1307C>A ENSP00000430767.1:p.Thr436Asn
NM_000843.3:c.1307C>A NP_000834.2:p.Thr436Asn
XR_941310.1:n.1470-765G>T
NM_000843.4:c.1307C>A MANE Select NP_000834.2:p.Thr436Asn
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