Canonical Allele Identifier: CA1624302989

Gene: GNMT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960615C= , CM000668.2:g.42960615C=	GRCh38
NC_000006.11:g.42928353C= , CM000668.1:g.42928353C=	GRCh37
NC_000006.10:g.43036331C=	NCBI36
NG_008396.1:g.4854C=

Transcript Alleles

HGVS	Amino-acid Change
XM_011514493.1:c.-13-1597C=	XP_011512795.1:n.-13-1597C=
XM_011514494.1:c.-13-1597C=	XP_011512796.1:n.-13-1597C=
NM_001318856.1:c.9-1597C=	NP_001305785.1:n.9-1597C=
NM_001318857.1:c.152-2147C=	NP_001305786.1:n.152-2147C=
NM_001318858.1:c.152-2147C=	NP_001305787.1:n.152-2147C=
NR_134890.1:n.690-2147C=
NR_134891.1:n.593-2147C=
NR_134892.1:n.593-1597C=
NM_001318856.2:c.9-1597C=	NP_001305785.1:n.9-1597C=
NM_001318857.2:c.152-2147C=	NP_001305786.1:n.152-2147C=
NM_001318858.2:c.152-2147C=	NP_001305787.1:n.152-2147C=
NR_134890.2:n.340-2147C=
NR_134891.2:n.243-2147C=
NR_134892.2:n.243-1597C=