Canonical Allele Identifier: CA11565842
Gene: METTL6 HGNC NCBI

Linked Data

dbSNP Id: rs6442522
gnomAD v2: 3-15440556-C-T
gnomAD v3: 3-15399049-C-T
gnomAD v4: 3-15399049-C-T
MyVariant Identifiers: chr3:g.15440556C>T (hg19) chr3:g.15399049C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15399049C>T , CM000665.2:g.15399049C>T GRCh38
NC_000003.11:g.15440556C>T , CM000665.1:g.15440556C>T GRCh37
NC_000003.10:g.15415560C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000443029.5:c.*11+12196G>A ENSP00000407613.1:n.*11+12196G>A
ENST00000458728.5:c.279-14862G>A
ENST00000584799.1:n.104+339G>A
XM_005264867.3:c.*11+12196G>A XP_005264924.1:n.*11+12196G>A
XM_006712972.2:c.618-14862G>A XP_006713035.1:n.618-14862G>A
XM_005264867.4:c.*11+12196G>A XP_005264924.1:n.*11+12196G>A
XM_006712972.4:c.618-14862G>A XP_006713035.1:n.618-14862G>A
XM_017005719.1:c.*11+12196G>A XP_016861208.1:n.*11+12196G>A
XM_017005723.1:c.483-14862G>A XP_016861212.1:n.483-14862G>A
XR_001740018.2:n.1056+12196G>A
XR_001740019.2:n.1198+12196G>A
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