Canonical Allele Identifier: CA2317700576
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401569C= , CM000681.2:g.1401569C= GRCh38
NC_000019.9:g.1401568C= , CM000681.1:g.1401568C= GRCh37
NC_000019.8:g.1352568C= NCBI36
NG_009785.1:g.4985G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447102.8:c.-93G= ENSP00000403536.2:n.-93G=
ENST00000447102.7:c.-93G= ENSP00000403536.2:n.-93G=
NM_000156.5:c.-93G= NP_000147.1:n.-93G=
NM_138924.2:c.-93G= NP_620279.1:n.-93G=