Canonical Allele Identifier: CA4883382
Gene: TG HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.132888141T>C
GRCh37 chr8:g.133900386T>C
gnomAD v2:
8:133900386 T / C
gnomAD v3:
8:132888141 T / C
gnomAD v4:
chr8-132888141-T-C
Joint Max Group AF 0.7546844 (EAS)
Genomes Max Group AF 0.74366432 (EAS)
Exomes Max Group AF 0.75398564 (EAS)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132888141T>C , CM000670.2:g.132888141T>C GRCh38
NC_000008.10:g.133900386T>C , CM000670.1:g.133900386T>C GRCh37
NC_000008.9:g.133969568T>C NCBI36
NG_015832.1:g.26182T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.2334T>C MANE Select ENSP00000220616.4:p.Pro778=
ENST00000220616.8:c.2334T>C ENSP00000220616.4:p.Pro778=
NM_003235.4:c.2334T>C NP_003226.4:p.Pro778=
XM_005251038.3:c.2334T>C XP_005251095.1:p.Pro778=
XM_005251040.3:c.2334T>C XP_005251097.1:p.Pro778=
XM_005251042.3:c.2334T>C XP_005251099.1:p.Pro778=
XM_005251043.3:c.2334T>C XP_005251100.1:p.Pro778=
XM_006716622.2:c.2334T>C XP_006716685.1:p.Pro778=
XM_005251038.4:c.2334T>C XP_005251095.1:p.Pro778=
XM_005251040.4:c.2334T>C XP_005251097.1:p.Pro778=
XM_005251042.4:c.2334T>C XP_005251099.1:p.Pro778=
XM_006716622.3:c.2334T>C XP_006716685.1:p.Pro778=
XM_017013793.1:c.2334T>C XP_016869282.1:p.Pro778=
XM_017013794.1:c.2334T>C XP_016869283.1:p.Pro778=
XM_017013795.1:c.2334T>C XP_016869284.1:p.Pro778=
XM_017013796.1:c.2334T>C XP_016869285.1:p.Pro778=
XM_017013797.1:c.2073T>C XP_016869286.1:p.Pro691=
XM_017013798.1:c.2334T>C XP_016869287.1:p.Pro778=
XM_017013799.1:c.2334T>C XP_016869288.1:p.Pro778=
XM_017013800.1:c.2334T>C XP_016869289.1:p.Pro778=
NM_003235.5:c.2334T>C MANE Select NP_003226.4:p.Pro778=
Search 100 bp 5'
Search 100 bp 3'