Canonical Allele Identifier: CA10917523
Gene: PRMT6 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.107058247G>A
GRCh37 chr1:g.107600869G>A
gnomAD v2:
1:107600869 G / A
gnomAD v3:
1:107058247 G / A
gnomAD v4:
chr1-107058247-G-A
Joint Max Group AF 0.18232901 (NFE)
Genomes Max Group AF 0.18618312 (NFE)
Exomes Max Group AF 0.17700016 (NFE)
dbSNP:
3791185
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.107058247G>A , CM000663.2:g.107058247G>A GRCh38
NC_000001.10:g.107600869G>A , CM000663.1:g.107600869G>A GRCh37
NC_000001.9:g.107402392G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000370078.2:c.*404G>A MANE Select ENSP00000359095.1:n.*404G>A
ENST00000649727.1:n.471+340G>A
ENST00000650338.1:c.1006+340G>A ENSP00000497826.1:n.1006+340G>A
ENST00000370078.1:c.*404G>A ENSP00000359095.1:n.*404G>A
NM_018137.2:c.*404G>A NP_060607.2:n.*404G>A
NM_018137.3:c.*404G>A MANE Select NP_060607.2:n.*404G>A
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