Canonical Allele Identifier: CA9731512
Gene: TGM6 HGNC NCBI

Linked Data

dbSNP Id: rs775445904
gnomAD v2: 20-2375073-A-G
gnomAD v4: 20-2394427-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2394427A>G , CM000682.2:g.2394427A>G GRCh38
NC_000020.10:g.2375073A>G , CM000682.1:g.2375073A>G GRCh37
NC_000020.9:g.2323073A>G NCBI36
NG_031917.1:g.18520A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000202625.7:c.8-25A>G MANE Select ENSP00000202625.2:n.8-25A>G
ENST00000202625.6:c.8-25A>G ENSP00000202625.2:n.8-25A>G
ENST00000381423.1:c.8-25A>G ENSP00000370831.1:n.8-25A>G
NM_001254734.1:c.8-25A>G NP_001241663.1:n.8-25A>G
NM_198994.2:c.8-25A>G NP_945345.2:n.8-25A>G
NM_001254734.2:c.8-25A>G NP_001241663.1:n.8-25A>G
NM_198994.3:c.8-25A>G MANE Select NP_945345.2:n.8-25A>G