Canonical Allele Identifier: CA362430177
Gene: GRM6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.178416091T>A (hg19) chr5:g.178989090T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178989090T>A , CM000667.2:g.178989090T>A GRCh38
NC_000005.9:g.178416091T>A , CM000667.1:g.178416091T>A GRCh37
NC_000005.8:g.178348697T>A NCBI36
NG_008105.1:g.11034A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000517717.3:c.1199A>T MANE Select ENSP00000430767.1:p.Lys400Met
ENST00000650031.1:c.1199A>T ENSP00000497110.1:p.Lys400Met
ENST00000231188.9:c.1199A>T ENSP00000231188.5:p.Lys400Met
ENST00000517717.1:c.1199A>T ENSP00000430767.1:p.Lys400Met
NM_000843.3:c.1199A>T NP_000834.2:p.Lys400Met
XR_941310.1:n.1470-657T>A
NM_000843.4:c.1199A>T MANE Select NP_000834.2:p.Lys400Met
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