Canonical Allele Identifier: CA364143455

Gene: GNMT

Linked Data

• MyVariant Identifiers: chr6:g.42928659C>G (hg19) ; chr6:g.42960921C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960921C>G , CM000668.2:g.42960921C>G	GRCh38
NC_000006.11:g.42928659C>G , CM000668.1:g.42928659C>G	GRCh37
NC_000006.10:g.43036637C>G	NCBI36
NG_008396.1:g.5160C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000372808.4:c.154C>G MANE Select	ENSP00000361894.3:p.Leu52Val
ENST00000372808.3:c.154C>G	ENSP00000361894.3:p.Leu52Val
NM_018960.4:c.154C>G	NP_061833.1:p.Leu52Val
XM_011514493.1:c.-13-1291C>G	XP_011512795.1:n.-13-1291C>G
XM_011514494.1:c.-13-1291C>G	XP_011512796.1:n.-13-1291C>G
NM_001318856.1:c.9-1291C>G	NP_001305785.1:n.9-1291C>G
NM_001318857.1:c.152-1841C>G	NP_001305786.1:n.152-1841C>G
NM_001318858.1:c.152-1841C>G	NP_001305787.1:n.152-1841C>G
NM_001318865.1:c.154C>G	NP_001305794.1:p.Leu52Val
NM_018960.5:c.154C>G	NP_061833.1:p.Leu52Val
NR_134890.1:n.690-1841C>G
NR_134891.1:n.593-1841C>G
NR_134892.1:n.593-1291C>G
NR_134899.1:n.168C>G
NM_018960.6:c.154C>G MANE Select	NP_061833.1:p.Leu52Val
NM_001318856.2:c.9-1291C>G	NP_001305785.1:n.9-1291C>G
NM_001318857.2:c.152-1841C>G	NP_001305786.1:n.152-1841C>G
NM_001318858.2:c.152-1841C>G	NP_001305787.1:n.152-1841C>G
NM_001318865.2:c.154C>G	NP_001305794.1:p.Leu52Val
NR_134890.2:n.340-1841C>G
NR_134891.2:n.243-1841C>G
NR_134892.2:n.243-1291C>G
NR_134899.2:n.168C>G