Canonical Allele Identifier: CA2576548801
Gene: GAMT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401549C>T , CM000681.2:g.1401549C>T GRCh38
NC_000019.9:g.1401548C>T , CM000681.1:g.1401548C>T GRCh37
NC_000019.8:g.1352548C>T NCBI36
NG_009785.1:g.5005G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000447102.8:c.-73G>A ENSP00000403536.2:n.-73G>A
ENST00000447102.7:c.-73G>A ENSP00000403536.2:n.-73G>A
NM_000156.5:c.-73G>A NP_000147.1:n.-73G>A
NM_138924.2:c.-73G>A NP_620279.1:n.-73G>A
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