Canonical Allele Identifier: CA70594182

Gene: METTL6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15389936C>T , CM000665.2:g.15389936C>T	GRCh38
NC_000003.11:g.15431443C>T , CM000665.1:g.15431443C>T	GRCh37
NC_000003.10:g.15406447C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443029.5:c.*12-5749G>A	ENSP00000407613.1:n.*12-5749G>A
ENST00000458728.5:c.279-5749G>A
ENST00000584799.1:n.105-5363G>A
XM_005264867.3:c.*12-5749G>A	XP_005264924.1:n.*12-5749G>A
XM_006712972.2:c.618-5749G>A	XP_006713035.1:n.618-5749G>A
XM_005264867.4:c.*12-5749G>A	XP_005264924.1:n.*12-5749G>A
XM_006712972.4:c.618-5749G>A	XP_006713035.1:n.618-5749G>A
XM_017005719.1:c.*12-5749G>A	XP_016861208.1:n.*12-5749G>A
XM_017005723.1:c.483-5749G>A	XP_016861212.1:n.483-5749G>A
XR_001740018.2:n.1057-5749G>A
XR_001740019.2:n.1199-5749G>A