Canonical Allele Identifier: CA2813256152
Gene: GAMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401558G>C , CM000681.2:g.1401558G>C GRCh38
NC_000019.9:g.1401557G>C , CM000681.1:g.1401557G>C GRCh37
NC_000019.8:g.1352557G>C NCBI36
NG_009785.1:g.4996C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000447102.8:c.-82C>G ENSP00000403536.2:n.-82C>G
ENST00000447102.7:c.-82C>G ENSP00000403536.2:n.-82C>G
NM_000156.5:c.-82C>G NP_000147.1:n.-82C>G
NM_138924.2:c.-82C>G NP_620279.1:n.-82C>G