Canonical Allele Identifier: CA257893593
Gene: TGM1 HGNC NCBI

Linked Data

dbSNP Id: rs1018351816
gnomAD v2: 14-24725073-G-C
gnomAD v3: 14-24255867-G-C
gnomAD v4: 14-24255867-G-C
MyVariant Identifiers: chr14:g.24725073G>C (hg19) chr14:g.24255867G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.24255867G>C , CM000676.2:g.24255867G>C GRCh38
NC_000014.8:g.24725073G>C , CM000676.1:g.24725073G>C GRCh37
NC_000014.7:g.23794913G>C NCBI36
NG_007150.1:g.12300C>G
NG_007150.2:g.12300C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206765.11:c.1491+122C>G MANE Select ENSP00000206765.6:n.1491+122C>G
ENST00000206765.10:c.1491+122C>G ENSP00000206765.6:n.1491+122C>G
ENST00000544573.5:c.165+122C>G ENSP00000439446.1:n.165+122C>G
ENST00000559136.1:c.564+122C>G ENSP00000453337.1:n.564+122C>G
NM_000359.2:c.1491+122C>G NP_000350.1:n.1491+122C>G
NM_000359.3:c.1491+122C>G MANE Select NP_000350.1:n.1491+122C>G
Search 100 bp 5'
Search 100 bp 3'