Canonical Allele Identifier: CA1624303053
Gene: GNMT HGNC NCBI

Linked Data

dbSNP Id: rs1769318389
gnomAD v3: 6-42960669-C-T
gnomAD v4: 6-42960669-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42960669C>T , CM000668.2:g.42960669C>T GRCh38
NC_000006.11:g.42928407C>T , CM000668.1:g.42928407C>T GRCh37
NC_000006.10:g.43036385C>T NCBI36
NG_008396.1:g.4908C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011514493.1:c.-13-1543C>T XP_011512795.1:n.-13-1543C>T
XM_011514494.1:c.-13-1543C>T XP_011512796.1:n.-13-1543C>T
NM_001318856.1:c.9-1543C>T NP_001305785.1:n.9-1543C>T
NM_001318857.1:c.152-2093C>T NP_001305786.1:n.152-2093C>T
NM_001318858.1:c.152-2093C>T NP_001305787.1:n.152-2093C>T
NR_134890.1:n.690-2093C>T
NR_134891.1:n.593-2093C>T
NR_134892.1:n.593-1543C>T
NM_001318856.2:c.9-1543C>T NP_001305785.1:n.9-1543C>T
NM_001318857.2:c.152-2093C>T NP_001305786.1:n.152-2093C>T
NM_001318858.2:c.152-2093C>T NP_001305787.1:n.152-2093C>T
NR_134890.2:n.340-2093C>T
NR_134891.2:n.243-2093C>T
NR_134892.2:n.243-1543C>T