Canonical Allele Identifier: CA450252129

Gene: GNMT

Linked Data

• MyVariant Identifiers: chr6:g.42928562G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960824G>C , CM000668.2:g.42960824G>C	GRCh38
NC_000006.11:g.42928562G>C , CM000668.1:g.42928562G>C	GRCh37
NC_000006.10:g.43036540G>C	NCBI36
NG_008396.1:g.5063G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372808.4:c.57G>C MANE Select	ENSP00000361894.3:p.Pro19=
ENST00000372808.3:c.57G>C	ENSP00000361894.3:p.Pro19=
NM_018960.4:c.57G>C	NP_061833.1:p.Pro19=
XM_011514493.1:c.-13-1388G>C	XP_011512795.1:n.-13-1388G>C
XM_011514494.1:c.-13-1388G>C	XP_011512796.1:n.-13-1388G>C
NM_001318856.1:c.9-1388G>C	NP_001305785.1:n.9-1388G>C
NM_001318857.1:c.152-1938G>C	NP_001305786.1:n.152-1938G>C
NM_001318858.1:c.152-1938G>C	NP_001305787.1:n.152-1938G>C
NM_001318865.1:c.57G>C	NP_001305794.1:p.Pro19=
NM_018960.5:c.57G>C	NP_061833.1:p.Pro19=
NR_134890.1:n.690-1938G>C
NR_134891.1:n.593-1938G>C
NR_134892.1:n.593-1388G>C
NR_134899.1:n.71G>C
NM_018960.6:c.57G>C MANE Select	NP_061833.1:p.Pro19=
NM_001318856.2:c.9-1388G>C	NP_001305785.1:n.9-1388G>C
NM_001318857.2:c.152-1938G>C	NP_001305786.1:n.152-1938G>C
NM_001318858.2:c.152-1938G>C	NP_001305787.1:n.152-1938G>C
NM_001318865.2:c.57G>C	NP_001305794.1:p.Pro19=
NR_134890.2:n.340-1938G>C
NR_134891.2:n.243-1938G>C
NR_134892.2:n.243-1388G>C
NR_134899.2:n.71G>C