Canonical Allele Identifier: CA509385713
Gene: TGM6 HGNC NCBI

Linked Data

dbSNP Id: rs1158581269
gnomAD v2: 20-2375068-G-T
gnomAD v3: 20-2394422-G-T
gnomAD v4: 20-2394422-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.2394422G>T , CM000682.2:g.2394422G>T GRCh38
NC_000020.10:g.2375068G>T , CM000682.1:g.2375068G>T GRCh37
NC_000020.9:g.2323068G>T NCBI36
NG_031917.1:g.18515G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000202625.7:c.8-30G>T MANE Select ENSP00000202625.2:n.8-30G>T
ENST00000202625.6:c.8-30G>T ENSP00000202625.2:n.8-30G>T
ENST00000381423.1:c.8-30G>T ENSP00000370831.1:n.8-30G>T
NM_001254734.1:c.8-30G>T NP_001241663.1:n.8-30G>T
NM_198994.2:c.8-30G>T NP_945345.2:n.8-30G>T
NM_001254734.2:c.8-30G>T NP_001241663.1:n.8-30G>T
NM_198994.3:c.8-30G>T MANE Select NP_945345.2:n.8-30G>T