Canonical Allele Identifier: CA14839170
Gene: TGM2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38163217G>T , CM000682.2:g.38163217G>T GRCh38
NC_000020.10:g.36791619G>T , CM000682.1:g.36791619G>T GRCh37
NC_000020.9:g.36225033G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361475.7:c.11-1618C>A MANE Select ENSP00000355330.2:n.11-1618C>A
ENST00000361475.6:c.11-1618C>A ENSP00000355330.2:n.11-1618C>A
ENST00000373403.7:c.11-1618C>A ENSP00000362502.3:n.11-1618C>A
ENST00000453095.1:c.11-1618C>A ENSP00000387642.1:n.11-1618C>A
ENST00000468262.5:n.95-1618C>A
ENST00000474777.1:n.72-1618C>A
NM_004613.2:c.11-1618C>A NP_004604.2:n.11-1618C>A
NM_198951.1:c.11-1618C>A NP_945189.1:n.11-1618C>A
XM_011529028.1:c.11-1618C>A XP_011527330.1:n.11-1618C>A
XM_011529029.1:c.11-1618C>A XP_011527331.1:n.11-1618C>A
NM_001323316.1:c.11-1618C>A NP_001310245.1:n.11-1618C>A
NM_001323317.1:c.11-1618C>A NP_001310246.1:n.11-1618C>A
NM_001323318.1:c.10+1972C>A NP_001310247.1:n.10+1972C>A
NM_004613.3:c.11-1618C>A NP_004604.2:n.11-1618C>A
NM_198951.2:c.11-1618C>A NP_945189.1:n.11-1618C>A
XR_001754586.1:n.589-24C>A
NM_004613.4:c.11-1618C>A MANE Select NP_004604.2:n.11-1618C>A
NM_001323316.2:c.11-1618C>A NP_001310245.1:n.11-1618C>A
NM_001323317.2:c.11-1618C>A NP_001310246.1:n.11-1618C>A
NM_001323318.2:c.10+1972C>A NP_001310247.1:n.10+1972C>A
NM_198951.3:c.11-1618C>A NP_945189.1:n.11-1618C>A
Search 100 bp 5'
Search 100 bp 3'