Canonical Allele Identifier: CA2317700561
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401554G= , CM000681.2:g.1401554G= GRCh38
NC_000019.9:g.1401553G= , CM000681.1:g.1401553G= GRCh37
NC_000019.8:g.1352553G= NCBI36
NG_009785.1:g.5000C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447102.8:c.-78C= ENSP00000403536.2:n.-78C=
ENST00000447102.7:c.-78C= ENSP00000403536.2:n.-78C=
NM_000156.5:c.-78C= NP_000147.1:n.-78C=
NM_138924.2:c.-78C= NP_620279.1:n.-78C=