Canonical Allele Identifier: CA2123832970
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1594568765

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24256282A>G , CM000676.2:g.24256282A>G GRCh38
NC_000014.8:g.24725488A>G , CM000676.1:g.24725488A>G GRCh37
NC_000014.7:g.23795328A>G NCBI36
NG_007150.1:g.11885T>C
NG_007150.2:g.11885T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1403-205T>C MANE Select ENSP00000206765.6:n.1403-205T>C
ENST00000206765.10:c.1403-205T>C ENSP00000206765.6:n.1403-205T>C
ENST00000544573.5:c.77-205T>C ENSP00000439446.1:n.77-205T>C
ENST00000559136.1:c.476-205T>C ENSP00000453337.1:n.476-205T>C
NM_000359.2:c.1403-205T>C NP_000350.1:n.1403-205T>C
NM_000359.3:c.1403-205T>C MANE Select NP_000350.1:n.1403-205T>C