Canonical Allele Identifier: CA2123854763
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs999298786
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259503T>G , CM000676.2:g.24259503T>G GRCh38
NC_000014.8:g.24728709T>G , CM000676.1:g.24728709T>G GRCh37
NC_000014.7:g.23798549T>G NCBI36
NG_007150.1:g.8664A>C
NG_007150.2:g.8664A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.984+201A>C MANE Select ENSP00000206765.6:n.984+201A>C
ENST00000206765.10:c.984+201A>C ENSP00000206765.6:n.984+201A>C
ENST00000544573.5:c.-28-1115A>C ENSP00000439446.1:n.-28-1115A>C
ENST00000559136.1:c.57+201A>C ENSP00000453337.1:n.57+201A>C
NM_000359.2:c.984+201A>C NP_000350.1:n.984+201A>C
NM_000359.3:c.984+201A>C MANE Select NP_000350.1:n.984+201A>C
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