Canonical Allele Identifier: CA2123854486
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs2040781228

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24258915T>C , CM000676.2:g.24258915T>C GRCh38
NC_000014.8:g.24728121T>C , CM000676.1:g.24728121T>C GRCh37
NC_000014.7:g.23797961T>C NCBI36
NG_007150.1:g.9252A>G
NG_007150.2:g.9252A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1159+160A>G MANE Select ENSP00000206765.6:n.1159+160A>G
ENST00000206765.10:c.1159+160A>G ENSP00000206765.6:n.1159+160A>G
ENST00000544573.5:c.-28-527A>G ENSP00000439446.1:n.-28-527A>G
ENST00000559136.1:c.232+160A>G ENSP00000453337.1:n.232+160A>G
NM_000359.2:c.1159+160A>G NP_000350.1:n.1159+160A>G
NM_000359.3:c.1159+160A>G MANE Select NP_000350.1:n.1159+160A>G