Canonical Allele Identifier: CA448027893
Gene: GRM6 HGNC NCBI

Linked Data

dbSNP Id: rs1484670886
gnomAD v4: 5-178994537-C-G
MyVariant Identifiers: chr5:g.178421538C>G (hg19) chr5:g.178994537C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.178994537C>G , CM000667.2:g.178994537C>G GRCh38
NC_000005.9:g.178421538C>G , CM000667.1:g.178421538C>G GRCh37
NC_000005.8:g.178354144C>G NCBI36
NG_008105.1:g.5587G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000517717.3:c.408G>C MANE Select ENSP00000430767.1:p.Pro136=
ENST00000650031.1:c.408G>C ENSP00000497110.1:p.Pro136=
ENST00000231188.9:c.408G>C ENSP00000231188.5:p.Pro136=
ENST00000517717.1:c.408G>C ENSP00000430767.1:p.Pro136=
NM_000843.3:c.408G>C NP_000834.2:p.Pro136=
NM_000843.4:c.408G>C MANE Select NP_000834.2:p.Pro136=
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