Linked Data
dbSNP Id:
rs1214300720
gnomAD v3:
1-109736817-A-ACT
gnomAD v4:
1-109736817-A-ACT
MyVariant Identifiers:
chr1:g.110279439_110279440insCT (hg19)
chr1:g.109736817_109736818insCT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109736821_109736822dup , CM000663.2:g.109736821_109736822dup | GRCh38 |
| NC_000001.10:g.110279443_110279444dup , CM000663.1:g.110279443_110279444dup | GRCh37 |
| NC_000001.9:g.110080966_110080967dup | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.*252_*253dup (GSTM3) MANE Select | ENSP00000354357.2:n.*252_*253dup | |
| ENST00000256594.7:c.*252_*253dup (GSTM3) | ENSP00000256594.3:n.*252_*253dup | |
| ENST00000361066.6:c.*252_*253dup (GSTM3) | ENSP00000354357.2:n.*252_*253dup | |
| ENST00000429410.2:n.82+24473_82+24474dup (GSTM5) | ||
| NM_000849.4:c.*252_*253dup (GSTM3) | NP_000840.2:n.*252_*253dup | |
| NR_024537.1:n.1164_1165dup (GSTM3) | ||
| NM_000849.5:c.*252_*253dup (GSTM3) MANE Select | NP_000840.2:n.*252_*253dup | |
| NR_024537.2:n.1164_1165dup (GSTM3) |