Canonical Allele Identifier: CA450252167

Gene: GNMT

Linked Data

• MyVariant Identifiers: chr6:g.42928622C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960884C>T , CM000668.2:g.42960884C>T	GRCh38
NC_000006.11:g.42928622C>T , CM000668.1:g.42928622C>T	GRCh37
NC_000006.10:g.43036600C>T	NCBI36
NG_008396.1:g.5123C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.117C>T MANE Select	ENSP00000361894.3:p.Arg39=
ENST00000372808.3:c.117C>T	ENSP00000361894.3:p.Arg39=
NM_018960.4:c.117C>T	NP_061833.1:p.Arg39=
XM_011514493.1:c.-13-1328C>T	XP_011512795.1:n.-13-1328C>T
XM_011514494.1:c.-13-1328C>T	XP_011512796.1:n.-13-1328C>T
NM_001318856.1:c.9-1328C>T	NP_001305785.1:n.9-1328C>T
NM_001318857.1:c.152-1878C>T	NP_001305786.1:n.152-1878C>T
NM_001318858.1:c.152-1878C>T	NP_001305787.1:n.152-1878C>T
NM_001318865.1:c.117C>T	NP_001305794.1:p.Arg39=
NM_018960.5:c.117C>T	NP_061833.1:p.Arg39=
NR_134890.1:n.690-1878C>T
NR_134891.1:n.593-1878C>T
NR_134892.1:n.593-1328C>T
NR_134899.1:n.131C>T
NM_018960.6:c.117C>T MANE Select	NP_061833.1:p.Arg39=
NM_001318856.2:c.9-1328C>T	NP_001305785.1:n.9-1328C>T
NM_001318857.2:c.152-1878C>T	NP_001305786.1:n.152-1878C>T
NM_001318858.2:c.152-1878C>T	NP_001305787.1:n.152-1878C>T
NM_001318865.2:c.117C>T	NP_001305794.1:p.Arg39=
NR_134890.2:n.340-1878C>T
NR_134891.2:n.243-1878C>T
NR_134892.2:n.243-1328C>T
NR_134899.2:n.131C>T