Linked Data
ClinVar Variation Id:
2794417
ClinVar RCV Id:
RCV003672828
dbSNP Id:
rs1685809660
gnomAD v4:
2-172469202-T-C
MyVariant Identifiers:
chr2:g.173333930T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.172469202T>C , CM000664.2:g.172469202T>C | GRCh38 |
| NC_000002.11:g.173333930T>C , CM000664.1:g.173333930T>C | GRCh37 |
| NC_000002.10:g.173042176T>C | NCBI36 |
| NG_008853.1:g.46617T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264107.12:c.465T>C (ITGA6) | ENSP00000264107.8:p.Tyr155= | |
| ENST00000442250.6:c.465T>C (ITGA6) MANE Plus Clinical | ENSP00000406694.1:p.Tyr155= | |
| ENST00000684293.1:c.465T>C (ITGA6) MANE Select | ENSP00000508249.1:p.Tyr155= | |
| ENST00000409080.6:c.465T>C (ITGA6) | ENSP00000386896.1:p.Tyr155= | |
| ENST00000264107.11:c.465T>C (ITGA6) | ENSP00000264107.7:p.Tyr155= | |
| ENST00000409080.5:c.465T>C (ITGA6) | ENSP00000386896.1:p.Tyr155= | |
| ENST00000409532.5:c.123T>C (ITGA6) | ENSP00000386614.1:p.Tyr41= | |
| ENST00000412899.5:c.123T>C (ITGA6) | ENSP00000413470.1:p.Tyr41= | |
| ENST00000442250.5:c.465T>C (ITGA6) | ENSP00000406694.1:p.Tyr155= | |
| ENST00000458358.5:c.465T>C (ITGA6) | ENSP00000394169.1:p.Tyr155= | |
| ENST00000497107.1:n.205T>C (ITGA6) | ||
| NM_000210.2:c.465T>C (ITGA6) | NP_000201.2:p.Tyr155= | |
| NM_000210.3:c.465T>C (ITGA6) | NP_000201.2:p.Tyr155= | |
| NM_001079818.1:c.465T>C (ITGA6) | NP_001073286.1:p.Tyr155= | |
| NM_001079818.2:c.465T>C (ITGA6) | NP_001073286.1:p.Tyr155= | |
| NM_001316306.1:c.123T>C (ITGA6) | NP_001303235.1:p.Tyr41= | |
| XM_006712510.1:c.465T>C (ITGA6) | XP_006712573.1:p.Tyr155= | |
| XM_006712511.1:c.465T>C (ITGA6) | XP_006712574.1:p.Tyr155= | |
| NM_001365529.1:c.465T>C (ITGA6) | NP_001352458.1:p.Tyr155= | |
| NM_001365530.1:c.465T>C (ITGA6) | NP_001352459.1:p.Tyr155= | |
| XM_017004005.1:c.123T>C (ITGA6) | XP_016859494.1:p.Tyr41= | |
| XM_017004006.1:c.123T>C (ITGA6) | XP_016859495.1:p.Tyr41= | |
| XM_017004007.1:c.123T>C (ITGA6) | XP_016859496.1:p.Tyr41= | |
| XM_017004008.1:c.123T>C (ITGA6) | XP_016859497.1:p.Tyr41= | |
| XR_001739781.1:n.410-4628A>G (ITGA6-AS1) | ||
| XR_001739782.1:n.410-3181A>G (ITGA6-AS1) | ||
| XR_001739784.1:n.410-3181A>G (ITGA6-AS1) | ||
| XR_001739785.1:n.410-3181A>G (ITGA6-AS1) | ||
| XR_001739786.1:n.521-3181A>G (ITGA6-AS1) | ||
| XR_001739788.1:n.505-4628A>G (ITGA6-AS1) | ||
| NM_001079818.3:c.465T>C (ITGA6) | NP_001073286.1:p.Tyr155= | |
| NM_000210.4:c.465T>C (ITGA6) MANE Select | NP_000201.2:p.Tyr155= | |
| NM_001316306.2:c.123T>C (ITGA6) | NP_001303235.1:p.Tyr41= | |
| NM_001365529.2:c.465T>C (ITGA6) | NP_001352458.1:p.Tyr155= | |
| NM_001365530.2:c.465T>C (ITGA6) | NP_001352459.1:p.Tyr155= | |
| NM_001394928.1:c.465T>C (ITGA6) MANE Plus Clinical | NP_001381857.1:p.Tyr155= |