Canonical Allele Identifier: CA824891788

Gene: GNMT

Linked Data

• dbSNP Id: rs1465442909
• gnomAD v4: 6-42960732-C-A
• MyVariant Identifiers: chr6:g.42928470C>A (hg19) ; chr6:g.42960732C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42960732C>A , CM000668.2:g.42960732C>A	GRCh38
NC_000006.11:g.42928470C>A , CM000668.1:g.42928470C>A	GRCh37
NC_000006.10:g.43036448C>A	NCBI36
NG_008396.1:g.4971C>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011514493.1:c.-13-1480C>A	XP_011512795.1:n.-13-1480C>A
XM_011514494.1:c.-13-1480C>A	XP_011512796.1:n.-13-1480C>A
NM_001318856.1:c.9-1480C>A	NP_001305785.1:n.9-1480C>A
NM_001318857.1:c.152-2030C>A	NP_001305786.1:n.152-2030C>A
NM_001318858.1:c.152-2030C>A	NP_001305787.1:n.152-2030C>A
NR_134890.1:n.690-2030C>A
NR_134891.1:n.593-2030C>A
NR_134892.1:n.593-1480C>A
NM_001318856.2:c.9-1480C>A	NP_001305785.1:n.9-1480C>A
NM_001318857.2:c.152-2030C>A	NP_001305786.1:n.152-2030C>A
NM_001318858.2:c.152-2030C>A	NP_001305787.1:n.152-2030C>A
NR_134890.2:n.340-2030C>A
NR_134891.2:n.243-2030C>A
NR_134892.2:n.243-1480C>A