Canonical Allele Identifier: CA257898340
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1034943705
gnomAD v3: 14-24258916-C-T
gnomAD v4: 14-24258916-C-T
MyVariant Identifiers: chr14:g.24728122C>T (hg19) chr14:g.24258916C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24258916C>T , CM000676.2:g.24258916C>T GRCh38
NC_000014.8:g.24728122C>T , CM000676.1:g.24728122C>T GRCh37
NC_000014.7:g.23797962C>T NCBI36
NG_007150.1:g.9251G>A
NG_007150.2:g.9251G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1159+159G>A MANE Select ENSP00000206765.6:n.1159+159G>A
ENST00000206765.10:c.1159+159G>A ENSP00000206765.6:n.1159+159G>A
ENST00000544573.5:c.-28-528G>A ENSP00000439446.1:n.-28-528G>A
ENST00000559136.1:c.232+159G>A ENSP00000453337.1:n.232+159G>A
NM_000359.2:c.1159+159G>A NP_000350.1:n.1159+159G>A
NM_000359.3:c.1159+159G>A MANE Select NP_000350.1:n.1159+159G>A
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