Canonical Allele Identifier: CA448027923
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs2113347689
MyVariant Identifiers: chr5:g.178421568C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994567C>G , CM000667.2:g.178994567C>G GRCh38
NC_000005.9:g.178421568C>G , CM000667.1:g.178421568C>G GRCh37
NC_000005.8:g.178354174C>G NCBI36
NG_008105.1:g.5557G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.378G>C MANE Select ENSP00000430767.1:p.Val126=
ENST00000650031.1:c.378G>C ENSP00000497110.1:p.Val126=
ENST00000231188.9:c.378G>C ENSP00000231188.5:p.Val126=
ENST00000517717.1:c.378G>C ENSP00000430767.1:p.Val126=
NM_000843.3:c.378G>C NP_000834.2:p.Val126=
NM_000843.4:c.378G>C MANE Select NP_000834.2:p.Val126=
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Search 100 bp 3'