Canonical Allele Identifier: CA364143335

Gene: GNMT

Linked Data

• gnomAD v4: 6-42960863-G-C
• MyVariant Identifiers: chr6:g.42928601G>C (hg19) ; chr6:g.42960863G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960863G>C , CM000668.2:g.42960863G>C	GRCh38
NC_000006.11:g.42928601G>C , CM000668.1:g.42928601G>C	GRCh37
NC_000006.10:g.43036579G>C	NCBI36
NG_008396.1:g.5102G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372808.4:c.96G>C MANE Select	ENSP00000361894.3:p.Gln32His
ENST00000372808.3:c.96G>C	ENSP00000361894.3:p.Gln32His
NM_018960.4:c.96G>C	NP_061833.1:p.Gln32His
XM_011514493.1:c.-13-1349G>C	XP_011512795.1:n.-13-1349G>C
XM_011514494.1:c.-13-1349G>C	XP_011512796.1:n.-13-1349G>C
NM_001318856.1:c.9-1349G>C	NP_001305785.1:n.9-1349G>C
NM_001318857.1:c.152-1899G>C	NP_001305786.1:n.152-1899G>C
NM_001318858.1:c.152-1899G>C	NP_001305787.1:n.152-1899G>C
NM_001318865.1:c.96G>C	NP_001305794.1:p.Gln32His
NM_018960.5:c.96G>C	NP_061833.1:p.Gln32His
NR_134890.1:n.690-1899G>C
NR_134891.1:n.593-1899G>C
NR_134892.1:n.593-1349G>C
NR_134899.1:n.110G>C
NM_018960.6:c.96G>C MANE Select	NP_061833.1:p.Gln32His
NM_001318856.2:c.9-1349G>C	NP_001305785.1:n.9-1349G>C
NM_001318857.2:c.152-1899G>C	NP_001305786.1:n.152-1899G>C
NM_001318858.2:c.152-1899G>C	NP_001305787.1:n.152-1899G>C
NM_001318865.2:c.96G>C	NP_001305794.1:p.Gln32His
NR_134890.2:n.340-1899G>C
NR_134891.2:n.243-1899G>C
NR_134892.2:n.243-1349G>C
NR_134899.2:n.110G>C