Linked Data
dbSNP Id:
rs1364173128
gnomAD v2:
3-123038478-C-CGA
gnomAD v3:
3-123319631-C-CGA
gnomAD v4:
3-123319631-C-CGA
MyVariant Identifiers:
chr3:g.123038478_123038479insGA (hg19)
chr3:g.123319631_123319632insGA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.123319631_123319632insGA , CM000665.2:g.123319631_123319632insGA | GRCh38 |
| NC_000003.11:g.123038478_123038479insGA , CM000665.1:g.123038478_123038479insGA | GRCh37 |
| NC_000003.10:g.124521168_124521169insGA | NCBI36 |
| NG_033882.1:g.133914_133915insTC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000466617.6:c.933+42_933+43insTC | ENSP00000420082.2:n.933+42_933+43insTC | |
| ENST00000470367.2:c.1221+42_1221+43insTC | ENSP00000514541.1:n.1221+42_1221+43insTC | |
| ENST00000483566.2:c.933+42_933+43insTC | ENSP00000420252.2:n.933+42_933+43insTC | |
| ENST00000699714.1:c.933+42_933+43insTC | ENSP00000514539.1:n.933+42_933+43insTC | |
| ENST00000699715.1:c.933+42_933+43insTC | ENSP00000514540.1:n.933+42_933+43insTC | |
| ENST00000699716.1:c.933+42_933+43insTC | ENSP00000514542.1:n.933+42_933+43insTC | |
| ENST00000699718.1:c.2256+42_2256+43insTC | ENSP00000514543.1:n.2256+42_2256+43insTC | |
| ENST00000699719.1:n.515+42_515+43insTC | ||
| ENST00000462833.6:c.2256+42_2256+43insTC MANE Select | ENSP00000419361.1:n.2256+42_2256+43insTC | |
| ENST00000309879.9:c.1206+42_1206+43insTC | ENSP00000308685.5:n.1206+42_1206+43insTC | |
| ENST00000462833.5:c.2256+42_2256+43insTC | ENSP00000419361.1:n.2256+42_2256+43insTC | |
| ENST00000466617.5:c.933+42_933+43insTC | ENSP00000420082.1:n.933+42_933+43insTC | |
| ENST00000491190.5:c.1155+42_1155+43insTC | ENSP00000418537.1:n.1155+42_1155+43insTC | |
| NM_001199642.1:c.1206+42_1206+43insTC | NP_001186571.1:n.1206+42_1206+43insTC | |
| NM_183357.2:c.2256+42_2256+43insTC | NP_899200.1:n.2256+42_2256+43insTC | |
| XM_005247077.2:c.2256+42_2256+43insTC | XP_005247134.1:n.2256+42_2256+43insTC | |
| XM_005247078.1:c.1206+42_1206+43insTC | XP_005247135.1:n.1206+42_1206+43insTC | |
| XM_006713483.1:c.1155+42_1155+43insTC | XP_006713546.1:n.1155+42_1155+43insTC | |
| XM_006713484.1:c.933+42_933+43insTC | XP_006713547.1:n.933+42_933+43insTC | |
| XM_011512358.1:c.2256+42_2256+43insTC | XP_011510660.1:n.2256+42_2256+43insTC | |
| XM_011512359.1:c.1257+42_1257+43insTC | XP_011510661.1:n.1257+42_1257+43insTC | |
| XM_011512360.1:c.1167+42_1167+43insTC | XP_011510662.1:n.1167+42_1167+43insTC | |
| XM_011512361.1:c.933+42_933+43insTC | XP_011510663.1:n.933+42_933+43insTC | |
| XM_005247077.4:c.2256+42_2256+43insTC | XP_005247134.1:n.2256+42_2256+43insTC | |
| XM_011512359.2:c.1257+42_1257+43insTC | XP_011510661.1:n.1257+42_1257+43insTC | |
| XM_011512360.3:c.1167+42_1167+43insTC | XP_011510662.1:n.1167+42_1167+43insTC | |
| XM_017005638.1:c.1158+42_1158+43insTC | XP_016861127.1:n.1158+42_1158+43insTC | |
| XM_017005639.1:c.1158+42_1158+43insTC | XP_016861128.1:n.1158+42_1158+43insTC | |
| NM_001378259.1:c.2256+42_2256+43insTC | NP_001365188.1:n.2256+42_2256+43insTC | |
| NM_183357.3:c.2256+42_2256+43insTC MANE Select | NP_899200.1:n.2256+42_2256+43insTC |