Canonical Allele Identifier: CA389256343
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1355803764
gnomAD v2: 14-24725238-C-T
gnomAD v4: 14-24256032-C-T
MyVariant Identifiers: chr14:g.24725238C>T (hg19) chr14:g.24256032C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24256032C>T , CM000676.2:g.24256032C>T GRCh38
NC_000014.8:g.24725238C>T , CM000676.1:g.24725238C>T GRCh37
NC_000014.7:g.23795078C>T NCBI36
NG_007150.1:g.12135G>A
NG_007150.2:g.12135G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1448G>A MANE Select ENSP00000206765.6:p.Gly483Asp
ENST00000206765.10:c.1448G>A ENSP00000206765.6:p.Gly483Asp
ENST00000544573.5:c.122G>A ENSP00000439446.1:p.Gly41Asp
ENST00000559136.1:c.521G>A ENSP00000453337.1:p.Gly174Asp
NM_000359.2:c.1448G>A NP_000350.1:p.Gly483Asp
NM_000359.3:c.1448G>A MANE Select NP_000350.1:p.Gly483Asp
Search 100 bp 5'
Search 100 bp 3'