Linked Data
dbSNP Id:
rs775242685
ExAC:
1:110279726 CTTG / C
gnomAD v2:
1-110279726-CTTG-C
gnomAD v3:
1-109737104-CTTG-C
gnomAD v4:
1-109737104-CTTG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.109737111_109737113del , CM000663.2:g.109737111_109737113del | GRCh38 |
| NC_000001.10:g.110279733_110279735del , CM000663.1:g.110279733_110279735del | GRCh37 |
| NC_000001.9:g.110081256_110081258del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361066.7:c.642_644del (GSTM3) MANE Select | ENSP00000354357.2:p.Asn214del | |
| ENST00000256594.7:c.642_644del (GSTM3) | ENSP00000256594.3:p.Asn214del | |
| ENST00000361066.6:c.642_644del (GSTM3) | ENSP00000354357.2:p.Asn214del | |
| ENST00000429410.2:n.82+24763_82+24765del (GSTM5) | ||
| ENST00000476321.5:n.610_612del (GSTM3) | ||
| ENST00000486823.5:n.606_608del (GSTM3) | ||
| ENST00000488824.1:n.987_989del (GSTM3) | ||
| NM_000849.4:c.642_644del (GSTM3) | NP_000840.2:p.Asn214del | |
| NR_024537.1:n.876_878del (GSTM3) | ||
| XM_011541296.1:c.861_863del (GSTM3) | XP_011539598.1:p.Asn287del | |
| NM_000849.5:c.642_644del (GSTM3) MANE Select | NP_000840.2:p.Asn214del | |
| NR_024537.2:n.876_878del (GSTM3) |