Linked Data
ClinVar Variation Id:
332386
dbSNP Id:
rs147900066
ExAC:
2:173362697 C / T
gnomAD v2:
2-173362697-C-T
gnomAD v3:
2-172497969-C-T
gnomAD v4:
2-172497969-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.172497969C>T , CM000664.2:g.172497969C>T | GRCh38 |
| NC_000002.11:g.173362697C>T , CM000664.1:g.173362697C>T | GRCh37 |
| NC_000002.10:g.173070943C>T | NCBI36 |
| NG_008853.1:g.75384C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264107.12:c.2944-6C>T (ITGA6) | ENSP00000264107.8:n.2944-6C>T | |
| ENST00000442250.6:c.3106-6C>T (ITGA6) MANE Plus Clinical | ENSP00000406694.1:n.3106-6C>T | |
| ENST00000684293.1:c.2989-6C>T (ITGA6) MANE Select | ENSP00000508249.1:n.2989-6C>T | |
| ENST00000409080.6:c.2989-6C>T (ITGA6) | ENSP00000386896.1:n.2989-6C>T | |
| ENST00000264107.11:c.2989-6C>T (ITGA6) | ENSP00000264107.7:n.2989-6C>T | |
| ENST00000409080.5:c.2989-6C>T (ITGA6) | ENSP00000386896.1:n.2989-6C>T | |
| ENST00000409532.5:c.2632-6C>T (ITGA6) | ENSP00000386614.1:n.2632-6C>T | |
| ENST00000416789.1:c.490-6C>T (ITGA6) | ENSP00000388435.1:n.490-6C>T | |
| ENST00000442250.5:c.3106-6C>T (ITGA6) | ENSP00000406694.1:n.3106-6C>T | |
| ENST00000458358.5:c.2974-6C>T (ITGA6) | ENSP00000394169.1:n.2974-6C>T | |
| ENST00000475302.1:n.405-6C>T (ITGA6) | ||
| NM_000210.2:c.2989-6C>T (ITGA6) | NP_000201.2:n.2989-6C>T | |
| NM_000210.3:c.2989-6C>T (ITGA6) | NP_000201.2:n.2989-6C>T | |
| NM_001079818.1:c.2989-6C>T (ITGA6) | NP_001073286.1:n.2989-6C>T | |
| NM_001079818.2:c.2989-6C>T (ITGA6) | NP_001073286.1:n.2989-6C>T | |
| NM_001316306.1:c.2632-6C>T (ITGA6) | NP_001303235.1:n.2632-6C>T | |
| XM_006712510.1:c.2944-6C>T (ITGA6) | XP_006712573.1:n.2944-6C>T | |
| XM_006712511.1:c.2944-6C>T (ITGA6) | XP_006712574.1:n.2944-6C>T | |
| NM_001365529.1:c.2944-6C>T (ITGA6) | NP_001352458.1:n.2944-6C>T | |
| NM_001365530.1:c.2944-6C>T (ITGA6) | NP_001352459.1:n.2944-6C>T | |
| XM_017004005.1:c.2647-6C>T (ITGA6) | XP_016859494.1:n.2647-6C>T | |
| XM_017004006.1:c.2602-6C>T (ITGA6) | XP_016859495.1:n.2602-6C>T | |
| XM_017004007.1:c.2647-6C>T (ITGA6) | XP_016859496.1:n.2647-6C>T | |
| XM_017004008.1:c.2602-6C>T (ITGA6) | XP_016859497.1:n.2602-6C>T | |
| XR_001739781.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739782.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739783.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739784.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739785.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739786.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739787.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739788.1:n.268-1743G>A (ITGA6-AS1) | ||
| XR_001739789.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739790.1:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739791.2:n.268-2453G>A (ITGA6-AS1) | ||
| XR_001739792.2:n.268-2453G>A (ITGA6-AS1) | ||
| NM_001079818.3:c.2989-6C>T (ITGA6) | NP_001073286.1:n.2989-6C>T | |
| NM_000210.4:c.2989-6C>T (ITGA6) MANE Select | NP_000201.2:n.2989-6C>T | |
| NM_001316306.2:c.2632-6C>T (ITGA6) | NP_001303235.1:n.2632-6C>T | |
| NM_001365529.2:c.2944-6C>T (ITGA6) | NP_001352458.1:n.2944-6C>T | |
| NM_001365530.2:c.2944-6C>T (ITGA6) | NP_001352459.1:n.2944-6C>T | |
| NM_001394928.1:c.3106-6C>T (ITGA6) MANE Plus Clinical | NP_001381857.1:n.3106-6C>T |