Canonical Allele Identifier: CA704351748
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs914790830
gnomAD v3: 14-24259423-C-T
gnomAD v4: 14-24259423-C-T
MyVariant Identifiers: chr14:g.24728629C>T (hg19) chr14:g.24259423C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24259423C>T , CM000676.2:g.24259423C>T GRCh38
NC_000014.8:g.24728629C>T , CM000676.1:g.24728629C>T GRCh37
NC_000014.7:g.23798469C>T NCBI36
NG_007150.1:g.8744G>A
NG_007150.2:g.8744G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.985-174G>A MANE Select ENSP00000206765.6:n.985-174G>A
ENST00000206765.10:c.985-174G>A ENSP00000206765.6:n.985-174G>A
ENST00000544573.5:c.-28-1035G>A ENSP00000439446.1:n.-28-1035G>A
ENST00000559136.1:c.58-174G>A ENSP00000453337.1:n.58-174G>A
NM_000359.2:c.985-174G>A NP_000350.1:n.985-174G>A
NM_000359.3:c.985-174G>A MANE Select NP_000350.1:n.985-174G>A
Search 100 bp 5'
Search 100 bp 3'