Linked Data
dbSNP Id:
rs35344500
gnomAD v2:
6-32609525-A-C
gnomAD v3:
6-32641748-A-C
gnomAD v4:
6-32641748-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32641748A>C , CM000668.2:g.32641748A>C | GRCh38 |
| NC_000006.11:g.32609525A>C , CM000668.1:g.32609525A>C | GRCh37 |
| NC_000006.10:g.32717503A>C | NCBI36 |
| NG_032876.1:g.9343A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343139.11:c.331+190A>C MANE Select | ENSP00000339398.5:n.331+190A>C | |
| ENST00000343139.9:c.331+190A>C | ENSP00000339398.5:n.331+190A>C | |
| ENST00000374949.2:c.331+190A>C | ENSP00000364087.2:n.331+190A>C | |
| ENST00000395363.5:c.331+190A>C | ENSP00000378767.1:n.331+190A>C | |
| ENST00000460633.1:n.359+190A>C | ||
| ENST00000482745.5:c.*1163+190A>C | ENSP00000436546.1:n.*1163+190A>C | |
| ENST00000496318.5:c.331+190A>C | ENSP00000437302.1:n.331+190A>C | |
| NM_002122.3:c.331+190A>C | NP_002113.2:n.331+190A>C | |
| XM_006715079.2:c.331+190A>C | XP_006715142.1:n.331+190A>C | |
| XM_006715079.4:c.331+190A>C | XP_006715142.1:n.331+190A>C | |
| XR_001744085.1:n.86+840T>G | ||
| NM_002122.5:c.331+190A>C MANE Select | NP_002113.2:n.331+190A>C |