Canonical Allele Identifier: CA1088343348
Gene: GNMT HGNC NCBI

Linked Data

dbSNP Id: rs1769308500
gnomAD v3: 6-42960458-C-A
gnomAD v4: 6-42960458-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42960458C>A , CM000668.2:g.42960458C>A GRCh38
NC_000006.11:g.42928196C>A , CM000668.1:g.42928196C>A GRCh37
NC_000006.10:g.43036174C>A NCBI36
NG_008396.1:g.4697C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011514493.1:c.-13-1754C>A XP_011512795.1:n.-13-1754C>A
XM_011514494.1:c.-13-1754C>A XP_011512796.1:n.-13-1754C>A
NM_001318856.1:c.9-1754C>A NP_001305785.1:n.9-1754C>A
NM_001318857.1:c.152-2304C>A NP_001305786.1:n.152-2304C>A
NM_001318858.1:c.152-2304C>A NP_001305787.1:n.152-2304C>A
NR_134890.1:n.690-2304C>A
NR_134891.1:n.593-2304C>A
NR_134892.1:n.593-1754C>A
NM_001318856.2:c.9-1754C>A NP_001305785.1:n.9-1754C>A
NM_001318857.2:c.152-2304C>A NP_001305786.1:n.152-2304C>A
NM_001318858.2:c.152-2304C>A NP_001305787.1:n.152-2304C>A
NR_134890.2:n.340-2304C>A
NR_134891.2:n.243-2304C>A
NR_134892.2:n.243-1754C>A