Canonical Allele Identifier: CA824891666

Gene: GNMT

Linked Data

• dbSNP Id: rs1397304179
• MyVariant Identifiers: chr6:g.42928334T>C (hg19) ; chr6:g.42960596T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960596T>C , CM000668.2:g.42960596T>C	GRCh38
NC_000006.11:g.42928334T>C , CM000668.1:g.42928334T>C	GRCh37
NC_000006.10:g.43036312T>C	NCBI36
NG_008396.1:g.4835T>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011514493.1:c.-13-1616T>C	XP_011512795.1:n.-13-1616T>C
XM_011514494.1:c.-13-1616T>C	XP_011512796.1:n.-13-1616T>C
NM_001318856.1:c.9-1616T>C	NP_001305785.1:n.9-1616T>C
NM_001318857.1:c.152-2166T>C	NP_001305786.1:n.152-2166T>C
NM_001318858.1:c.152-2166T>C	NP_001305787.1:n.152-2166T>C
NR_134890.1:n.690-2166T>C
NR_134891.1:n.593-2166T>C
NR_134892.1:n.593-1616T>C
NM_001318856.2:c.9-1616T>C	NP_001305785.1:n.9-1616T>C
NM_001318857.2:c.152-2166T>C	NP_001305786.1:n.152-2166T>C
NM_001318858.2:c.152-2166T>C	NP_001305787.1:n.152-2166T>C
NR_134890.2:n.340-2166T>C
NR_134891.2:n.243-2166T>C
NR_134892.2:n.243-1616T>C