Canonical Allele Identifier: CA402997361
Gene: GAMT HGNC NCBI

Linked Data

gnomAD v4: 19-1399939-C-T
MyVariant Identifiers: chr19:g.1399938C>T (hg19) chr19:g.1399939C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399939C>T , CM000681.2:g.1399939C>T GRCh38
NC_000019.9:g.1399938C>T , CM000681.1:g.1399938C>T GRCh37
NC_000019.8:g.1350938C>T NCBI36
NG_009785.1:g.6615G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.182-1G>A MANE Select ENSP00000252288.1:n.182-1G>A
ENST00000447102.8:c.182-1G>A ENSP00000403536.2:n.182-1G>A
ENST00000640762.1:c.113-1G>A ENSP00000492031.1:n.113-1G>A
ENST00000252288.6:c.182-1G>A ENSP00000252288.1:n.182-1G>A
ENST00000447102.7:c.182-1G>A ENSP00000403536.2:n.182-1G>A
NM_000156.5:c.182-1G>A NP_000147.1:n.182-1G>A
NM_138924.2:c.182-1G>A NP_620279.1:n.182-1G>A
NM_000156.6:c.182-1G>A MANE Select NP_000147.1:n.182-1G>A
NM_138924.3:c.182-1G>A NP_620279.1:n.182-1G>A
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