Canonical Allele Identifier: CA362436695
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs2113347914
gnomAD v4: 5-178994658-A-G
MyVariant Identifiers: chr5:g.178421659A>G (hg19) chr5:g.178994658A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994658A>G , CM000667.2:g.178994658A>G GRCh38
NC_000005.9:g.178421659A>G , CM000667.1:g.178421659A>G GRCh37
NC_000005.8:g.178354265A>G NCBI36
NG_008105.1:g.5466T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.287T>C MANE Select ENSP00000430767.1:p.Leu96Pro
ENST00000650031.1:c.287T>C ENSP00000497110.1:p.Leu96Pro
ENST00000231188.9:c.287T>C ENSP00000231188.5:p.Leu96Pro
ENST00000517717.1:c.287T>C ENSP00000430767.1:p.Leu96Pro
NM_000843.3:c.287T>C NP_000834.2:p.Leu96Pro
NM_000843.4:c.287T>C MANE Select NP_000834.2:p.Leu96Pro
Search 100 bp 5'
Search 100 bp 3'