Canonical Allele Identifier: CA969359877
Gene: GATM HGNC NCBI

Linked Data

dbSNP Id: rs1889893738

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45393522T>C , CM000677.2:g.45393522T>C GRCh38
NC_000015.9:g.45685720T>C , CM000677.1:g.45685720T>C GRCh37
NC_000015.8:g.43473012T>C NCBI36
NG_011674.2:g.13796A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000458245.5:n.640+3400A>G
ENST00000527933.2:n.512+2645A>G
ENST00000560538.1:n.338+3400A>G
ENST00000561148.5:c.-319+3400A>G ENSP00000453860.1:n.-319+3400A>G
XM_011521450.1:c.31+3400A>G XP_011519752.1:n.31+3400A>G
NM_001321015.1:c.-395+3400A>G NP_001307944.1:n.-395+3400A>G
NM_001321015.2:c.-395+3400A>G NP_001307944.1:n.-395+3400A>G